Institut für Humangenetik

Universität Göttingen

28.2.2000

Publikationsliste

Jahrgänge 93 94 95 96 97 98 99

1993

Adham, I. M., Burkhardt, E., Benahmed, M., Engel, W.: Cloning of a cDNA for a novel insulin-like peptide of the testicular Leyding cells. The Journal of Biological Chemistry 268, 26668-26672 (1993)

Bartels, I., Hoppe-Sievert, B., Bockel, B., Herold, S., Caesar, J.: Adjustment formulare for maternal serum Alpha-Fetoprotein, human chorionic gonadotropin and unconjugated oestriol to maternal weight and smoking. Prenatal Diagnosis 13, 123-130 (1993)

Bartels, I.: Chromosomenanalyse genetisch bedingter Erkrankungen. Z. Allg. Med. 69, 883-887 (1993)

Braulke, I., Zoll, B.: Genetische Beratung in der Schwangerschaft. TW Gynäkologie 6, 127-130 (1993)

Braulke, I., Pruggmayer, M., Melloh, P., Hinney, B., Köstering, H., Günther, E.: Factor XII (Hageman) deficiency in women with habitual abortion: new subpopulation of recurrent aborters? Fertility and Sterility 59, 98-101 (1997)

Burfeind, P., Belgardt, B., Szpirer, C., Hoyer-Fender, S.: Structure and chromosomal assignment of a gene encoding the major protein of rat sperm outer dense fibres. Eur. J. Biochem. 216, 497-505 (1993)

Callen, D. F., Eyre, H., Lane, S., Shen, Y., Hansmann, I., Spinner, N., Zackai, E., McDonald-McGinn, D., Schuffenhauer, S., Wauters, J., Van Thienen, M-N., Van Roy, B., Sutherland, G. R., Haan, E. A.: High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype. J. Med. Genet. 30, 828-832 (1993)

Darscht, A.: Angeborene Klumpfüsse und Genetik. Z. Allg. Med. 69, 891-893 (1993)

Engel, W., Adham, I. M., Keime, S., Kremling, H., Schlösser, M., Nayernia, K.: The acrosin gene: structure, regulation and function. In: Serono Symposia Publication 97, 87-93 (1993)

Franke, U.-C.: Zur Genetik angeborener Herzerkrankungen. Z. Allg. Med. 69, 935-940 (1993)

Hansmann, I.: Der informierte Arzt. Gazette Medicale 14, 809-818 (1993)

Hofferbert, S., Burfeind, P., Hoyer-Fender, S., Lange, R., Haidl, G., Engel, W.: A homozygous deletion of 27 basepairs in the coding region of the human outer dense fiber protein gene does not result in a pathologic phenotype. Hum. Mol. Gen. 2, 2167-2170 (1993)

Jörgensen, G.: Auch im Alter: "Liebe ist die beste Medizin" Borsuye 19, 27 (1993)

Jörgensen, G.: Die Bürde des Menschen ist unantastbar . . . "Anpassungsstrategien" im Seniorenalter. Schleswig-Holsteinisches Ärzteblatt 46, 22-23 (1993)

Keith, T. P., Hansmann, I., Weissenbach, J.: Report of the committee on the genetic constitution of chromosome 20 Genome Priority Reports 1, 548-555 (1993)

Knobloch, O., Pelz, F., Wick, U., Nelson, D. L., Zoll, B.: Direct versus indirect molecular diagnosis of fragile X mental retardation in 40 German families at risk J. Med. Genet. 30, 193-197 (1993)

Knobloch, O., Zoll, B., Zerres, K., Brackmann, H.-H., Olek, K., Ludwig, M.: Recurrent mutations in the factor IX gene: founder effect or repeat de novo events. Hum. Genet. 92, 40-48 (1993)

Koch, M., C., Ricker, K., Otto, M., Wolf, F., Zoll, B., Lorenz, C., Steinmeyer, K., Jentsch, T. J.: Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker). J. Med. Genet. 30, 914-917 (1993)

Krawczak, M., Böhm, I., Nürnberg, P., Hampe, J., Hundrieser, J., Pöche, H., Peters, C., Slomski, R., Kwiatkowska, J., Nagy, M., Pöpper, A., Epplen, J. T., Schmidtke, J.: Paternity testing with oligonucleotide multilocus probe (CAC)₅/(GTG)₅: A multicenter study. Forensic Sc. Int. 59, 101-117 (1993)

Krawczak, M., Bockel, B.: The formal analysis of multilocus Dna fingerprints. In: DNA Fingerprinting: State of the Science, Pena, S. D. J., Chkreborty, R., Epplen, J., eds. 249-255, Birkhäuser Verlag, Basel (1993)

Krasemann, E. W.: Die Amyotrophe Lateralsklerose. Niedersächs. Ärzteblatt 19, 22-24 (1993)

Krasemann, E. W.: Atopische Erkrankungen und ihre Vererbung. Z. Allg. Med. 69, 888-890 (1993)

Krasemann, E. W.: Klinik und Genetik der Adrenoleukodystrophie. Niedersächs. Ärzteblatt 6, 27-28 (1993)

Krasemann, E. W., Krasemann, E. O., Bockel, B.: Verändern chronische Herzkrankheiten das Sexualverhalten? Herz/Kreisl. 25, 47-51 (1993)

Kreuz, F., Wittwer, B. H.: Del(2q) - cause of the wrinkly skin syndrome? Clin. Genet. 43, 132-138 (1993)

Kreuz, F.: Bericht von der 5. Tagung der Gesellschaft für Humangenetik e. V. (Würzburg 17. -20. März 1993) DHH Quartalszeitung 2, 20-21 (1993)

Kreuz, F.: Heredo-Ataxien - bekannt und verkannt? Ärzteblatt Sachsen-Anhalt 8, 537-538 (1993)

Kreuz, F.: Neurodegenerative Krankheitsbilder mit Demenz. Spätmanifestierende Erkrankungen des Zentralnervensystems - Klinik und Genetik (Teil 1) Z. Allg. Med. 69, 930-934 (1993)

Kreuz, F.: Psychotische Krankheitsbilder. Spätmanifestierende Erkrankungen des Zentralnervensystems - Klinik und Genetik (Teil 2). Z. Allg. Med. 69, 930-934 (1993)

Laccone, F.-A.: Krebs als genetisch mitbedingte Erkrankung. Z. Allg. Med. 69, 919-924 (1993)

Laccone, F-A., Zoll, B.: Zur Klinik und Genetik des Morbus Bechterew. Niedersächs. Ärzteblatt 7, 32-33 (1993)

Lange, R., Johannson, G., Engel, W.: Chromosome studies in in-vitro fertilization patients. Human Reprod. 8, 572-574 (1993)

Lange, R., Johannson, G., Hinney, B., Michelmann, H. W.: Zytogenetische Untersuchungen bei IVF-Patienten. Fertilität 9, 41-44 (1993)

Niemann-Seyde, S., Rehder, H., Zoll, B.: A case of full triploidy (69,XXX) of paternal origin with unusually long survival time. Clin. Genet. 43, 79-82 (1993)

Pelz, F.: Zur Molekulargenetik des Martin-Bell-Syndroms. Niedersächs. Ärzteblatt 15, 17-18 (1993)

Reiss, J., Ellermeyer, U., Rininsland, R., Ballhausen, P., Lenz, U., Wagner, S., Schlösser, M.: A comprehensive CFTR mutation analysis of German dystic fibrosis patients. Hum. Mol. Genet. 2, 809-811 (1993)

Reiss, J.: Would you sign your criticism? The Lancet 341, 1097 (1993)

Reiss, J., Ellermeyer, U., Schlösser, M., Fuhrmann, W., Drews, D., Posselt, H. G.: Two cystic fibrosis patients with the genotype G542X/G551D. Hum. Genet. 91, 78-79 (1993)

Reiss, J.: Möglichkeiten der DNA-Diagnostik. Z. Allg. Med. 69, 879-882 (1993)

Rothschild, C. B., Akots, G., Hayworth, R., Pettenati, M. J., Rao, N. P., Wood, P., Stolz, F.-M., Hansmann, I., Serino, K., Keith, T. P., Fajans, S., Bowden, D. W.: A genetic map of chromosome 20q12-q13.I: Multiple highly polymorphic microsatellite and RFLP markers linked to the Maturity-Onset Diabetes of the Young (MODY) Locus. Am. Journ. Hum. Genet. 52, 110-123 (1993)

Suren, A., Gröne, H. J., Kallerhoff, M., Weber, M. H., Zoll, B., Osmers, R.: Prenatal diagnosis of congenital nephrosis of the Finnish type (CNF) in the second trimester. Int. J. Gynecol. Obstet. 41, 165-170 (1993)

Schlüter, G., Schlicker, M., Engel, W.: A conserved 8bp motif (GCYATCAY) in the 3'utr of transition protein 2 as a putative target for a transcript stabilizing protein factor. Biochem. Biophys. Res. Commun. 197, 110-115 (1993)

Schnittger, S.,VGopal Rao, V. V. N., Abrahamson, M., Hansmann, I.: Cystatin C (CST3), the candidate gene for Hereditary Dystatin C Amyloid Angiopathy (HCCAA), and other members of the Cystatin gene family are clustered on chromosome 20p11.2. Genomics 16, 50-55 (1993)

Thies, U.: Genetik der Chorea Huntington. Nervenheilkunde 12, 59-62 (1993)

Thies, U. Zühlke, C.: Direkte DNA-Diagnostik bei Huntingtonscher Erkrankung. Deutsches Ärzteblatt 90, 2129-2130 (1993)

Thies, U., Bockel, B., Bochdalofsky, V.: Attitudes of neurologists, psychiatrists, and psychotherapists towards predictive testing for Huntington's disease in Germany. J. Med. Genet. 30, 1023-1027 (1993)

Thies, U., Bockel, B., Gerdes, B., Schröder, K.: Allele frequencies and linkage disequilibrium of polymorphic DNA markers of the Huntington disease region in the German population. Hum. Genet. 92, 593-597 (1993)

Wagner, M., Reiss, J.: The Cystic Fibrosis Gene. Adv. Genome Biol. 2, 69-98 (1993)

Will, K., Reiss, J., Dean, M., Schlösser, M., Slomski, R., Schmidtke, J., Stuhrmann, M.: CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553X. J. Med. Genet. 30, 833-837 (1993)

Willoh, R., Zühlke, C., Gerdes, B., Wiese, S., Thies, U.: PCR analysis of a three-allelic PvuII-RFLP at D4S127 closely linked to the Huntington disease locus. Clin. Genet. 43, 321-323 (1993)

Zoll, B., Wolf, J., Lensing-Hebben, D., Pruggmayer, M., Thorpe, B.: Trisomy 13 (Patau syndrome) with an 11-year survival. Clin. Genet. 43, 46-50 (1993)

Zoll, B.: Genetische Familienberatung. Z. Allg. Med. 69, 875-878 (1993)

Zühlke, C., Riess, O., Schröder, K., Siedlaczck, I., Epplen, J. T., Engel, W., Thies, U.: Expansion of the (CAG)_n repeat causing Huntington's disease in 352 Patients of German origin. Hum. Mol. Genet. 2, 1467-1469 (1993)

Zühlke, C., Thies, U.: Allele frequencies of DNA markers genetically linked to Friedreich Ataxia in the german population. Hum. Hered. 43, 78-81 (1993)

Zühlke, C., Riess, O., Bockel, B., Lange, H., Thies, U.: Mitotic stability and meiotic variability of the (CAG)_n repeat in the Huntington disease gene. Hum. Mol. Genet. 2, 2063-2067 (1993)

1994

Bartels, I., Caesar, J., Sancken, U.: Prenatal detection of X-linked ichthyosis by maternal serum screening for Down syndrome. Prenatal Diagnosis 14, 227-229 (1994)

Bartels, I., Bockel, B., Caesar, J., Krawczak, M., Thiele, M., Rauskolb, R.: Risk of fetal Down's syndrome based on maternal age and varying combinations ofmaternal serum markers. Archives of Gynecology and Obstetrics 255, 57-64 (1994)

Bartels, I., Sancken, U.: Pränataler Risikoindex für fetales Down Syndrom mit Serummarkern. Zeitschrift für Geburtshilfe und Perinatologie 198, 153-154 (1994)

Becker, P. E.: Eine Muskeldystrophie-Untersuchung vor mehr als 50 Jahren. Medizinische Genetik 3, 328-331 (1994)

Braulke, I., Zoll, B., Hartmann, H.: Hereditary pancreatitis - a case report. Zeitschrift für Gastroenterologie 32, 645-646 (1994)

Burfeind, P., Hoyer-Fender, S., Doenecke, D., Hochhuth, C., Engel, W.: Expression and chromosomal mapping of the gene encoding the human histone H1.1. Human Genetics 94, 633-639 (1994)

Burkhardt, E., Adham, I. M., Brosig, B., Gastmann, A., Mattei, M.-G., Engel, W.: Structural organization of the porcine and human genes coding for a Leydig cell-specific insuline-like peptide (LEY I-L) and chromosomal localization of the human gene (INSL3). Genomics 20, 13-19 (1994)

Burkhardt, E., Adham, I. M., Hobohm, U., Murphy, D., Sander, C., Engel, W.: A human cDNA coding for the Leydig insulin-like peptide (Ley I-L). Human Genetics 94, 91-94 (1994)

Caspari, D., Bartels, I., Rauskolb, R., Prange, G., Osmers, R., Eiben, B.: Discrepant karyotypes after second- and third-trimester combined placentacentesis/ amniocentesis. Prenatal Diagnosis 14, 569-576 (1994)

Cooper, D. N., Berg, L.-P., Kakkar, V. V., Reiss, J.: Ectopic (illegitimate) transcription: new possiblities for the analysis and diagnosis of human genetic disease. Annals of Medicine 26, 9-14 (1994)

Franke, U. C., Scambler, P. J., Löffler, C., Löns, P., Hanefeld, F., Zoll, B., Hansmann, I.: Interstitial deletion of 22q11 in DiGeorge syndrome detected by high resolution and molecular analysis. Clinical Genetics 46, 187-192 (1994)

Friedl, R., Adham, I. M., Rottman, O. J.: Physical mapping of bovine outer dense fiber gene (ODF) to chromosome BTA 14q23-24 in cattle. Mammalian Genome 5, 833-834 (1994)

Friedl, R., Adham, I. M., Rottmann, O. J.: Mapping of the gene encoding bovine preproacrosin (ACR) to chromosome BTA 5 region q35. Mammalian Genome 5, 830-831 (1994)

Giannakoudis, J., Mortazawi, M.-S., Pabst, B., Wrisch, A., Herlt, S., Hanefeld, F., Hansmann, I.: Allele loss for chromosome 17p13.3 markers in an unselected survey of type I lissencephaly. Medizinische Genetik 6, 89 (1994)

Giannakoudis, J., Mortazawi, M.-S., Wrisch, A., Färber, C., Herlt, S., Hanefeld, F., Hansmann, I.: Microdeletions of chromosome 17p13.3 markers in an unselected survey of probands with type I lissencephaly. American Journal of Human Genetics 55, A 11 (1994)

Hansmann, I., Keith, T. P.: Report of the committee on the genetic constitution of chromosome 20. In: Human Gene Mapping 1993. A Compendium. Cuticchia, A. J., Pearson, P. L. (Eds), John Hopkins University Press, Baltimore, 598-610 (1994)

Hansmann, I., von der Kammer, S., Löffler, C., Franke, Y., Paarmann, I., Schwiegk, C.; Herlt, S., Schröter, A., Manjunath, N. A., Goodship, J., LePaslier, D., Giannakoudis, J.: Cloning the Alagille syndrome region (AGSCR) at 20p11.23-p12.1 into yacs and identification of molecular deletions. American Journal of Human Genetics 55, A 259 (1994)

Hofferbert, S., Müller, J., Hinney, B., Köstering, H., Engel, W.: Molecular characterization of factor XII deficiency in women with habitual abortion and in Hageman trait subjects without clinical symptoms. 7th International Conference on Early Prenatal Diagnosis, Jerusalem, May, 22-27, 1994 Monduzzi Editore S. p. A., Bologna; Zakut, H., (Ed.), 223-226 (1994)

Hofferbert, S.: Genetische Einflüsse beim Alkoholismus (Teil 1): Das Verständnis der Erkrankung ist noch lückenhaft.Niedersächsisches Ärzteblatt 67, 43-44 (1994)

Hofferbert, S.: Genetische Einflüsse beim Alkoholismus (Teil 2): Adoptions- und Zwillingsstudien sollen neue Erkenntnisse bringen. Niedersächsisches Ärzteblatt 67, 15-16 (1994)

Hofferbert, S.: Genetische Einflüsse beim Alkoholismus (Teil 3): Die Suche möglicher Ursachen für die Erkrankung. Niedersächsisches Ärzteblatt 67, XX-XX (1994)

Horst-Sikorska, W., Zoll, B., Kwiatkowska, J., Willms, B., Kraszewski, A., Horst, ., Slomski, R.: Prevalence of beta allele of the insulin gene in type II diabetes mellitus. Human Genetics 93, 325-328 (1994)

Krawczak, M., Schmidtke, J., Epplen, J., Hansmann, I., Thies, U.: A multilocus DNA fingerprint with built-in security devices.Medicine, Science and Law 34, 256-262 (1994)

Kreuz, F. R., Pelz, F., Plate, I., Zoll, B.: Martin-Bell-Syndrom bei einem Mädchen - ein ungewöhnlicher, sporadischer Fall? Monatsschrift für Kinderheilkunde 142, 341-344 (1994)

Kreuz, F. R., Bockel, B.: Attitudes of persons at risk of Huntington's disease and their partners towards molecular genetic testing. Medizinische Genetik 6, 348 (1994)

Kreuz, F. R., Bockel, B.: Attitudes of persons at risk for Huntington's disease and their partners towards molecular genetic testing. Movement Disorders 9, 29 (1994)

Kwon, H. Y., Bultman, S. J., Löffler, C., Chen, W.-J., Furdon, P. J., Powell, J. G., Usala, A.-L., Wilkinson, W., Hansmann, I., Woychik, R. P.: Molecular structure and chromosomal mapping of the human homolog of the agouti gene.Proceedings National Academy of Sciences USA 91, 9760-9764 (1994)

Kynast, B., Marx, D., Schlicker, M., Schauer, A., Schmoll, H. J., Zoll, B., Poliwoda, H.: Alterations of HER-2, HER-3 and p53 genes in human breast cancer. Journal of Cancer Research and Clinical Oncology 120, R 38 (1994)

Löffler, C., Rao, V. V. N. G., Müllmann, S., Schnittger, S., Pastuszak, D., Schubert, S., Schröter, A., Hansmann, I.: Generation of a physical map of human chromosome 20 by FISH disclose complete homology with mouse chromosome 2. Medizinische Genetik 6, 120 (1994)

Meyer-Kleine, C., Otto, M., Zoll, B., Koch, M. C.: Molecular and genetic characterization of German families with paramyotonia congenita and demonstration of founder effect in Ravensberg families. Human Genetics 93, 707-710 (1994)

Müllmann, S., Löffler, S., Schwiegk, C., Franke, Y., LePaslier, D., Keith, T., Hansmann, I.: Physical mapping of the Alagille syndrome chromosome region (AGSCR) on chromosome 20p11.23-p12.1 using yeast artifical chromosomes and search for candidate genes. Medizinische Genetik 6, 87 (1994)

Murphy, D. B., Wiese, S., Burfeind, P., Schmundt, D., Mattei, M.-G., Schulz-Schaeffer, W., Thies, U.: Human brain factor 1, a new member of the fork head gene family. Genomics 21, 551-557 (1994)

Nayernia, K., Reim, K., Oberwinkler, H., Engel, W.: Diploid expression and translational regulation of rat acrosin gene. Biochemical and Biophysical Research Communications 202, 88-93 (1994)

Nayernia, K., Oberwinkler, H., Engel, W.: Developmental and translational regulation of the rat and mouse proacrosin gene expression. Genetics (Life Sci. Adv.) 12, 121-129 (1993)

Nayernia, K., Nieter, S., Kremling, H., Oberwinkler, H., Engel, W.: Functional and molecular characterization of the transcriptional regulatory region of the proacrosin gene. The Journal of Biological Chemistry 269, 32181-32186 (1994)

Neesen, J., Padmanabhan, S., Bünemann, H.: Tandemly arranged repeats of a novel highly charged 16-amino-acid motif representing the major component of the sperm-tail-specific axoneme-associated protein family Dhmst101 form extended à-helical rods within the extremely elongated spermatozoa of Drosophila hydei. European Journal of Biochemistry 225, 1089-1095 (1994)

Neesen, J., Bünemann, H., Heinlein, U. A. O.: The Drosophila hydei gene Dhmst101(1) encodes a testis-specific, repetitive, axoneme- associated protein with differential abundance in Y chromosomal deletion mutant flies. Developmental Biology 162, 414-425 (1994)

Paarmann, I., Giannakoudis, J., Herlt, S., Wrisch, A., Hansmann, I.: Search for molecular deletions in Alagille syndrome. Medizinische Genetik 6, 122 (1994)

Pabst, B., Hansmann, I.: Nondisjunction by failures in the molecular control of oocyte maturation. In: "Chromosomal alterations: Origin and significance", Obe, G., Natarajan, A. T. (Eds.): Chromosomal Alterations, Springer Verlag Heidelberg, 262-268 (1994)

Reiss, J., Rininsland, F.: An explanation for the constitutive exon 9 cassette splicing of the DMD gene. Human Molecular Genetics 3, 295-298 (1994)

Rettenberger, G., Adham, I. M., Engel, W., Klett, C., Hameister, H.: Assignment of the porcine transition protein TNP1 to chromosome 15q24-25 by fluorescence in situ hybridization (FISH). Mammalian Genome 5, 249-250 (1994)

Rettenberger, G., Burkhardt, E., Adham, I. M., Engel, W., Fries, R., Klett, C., Hameister, H.: Assignment of the Leydig insulin-like hormone to porcine chromosome 2q12-q13 by somatic cell hybrid analysis and fluorescence in situ hybridization. Mammalian Genome 5, 307-309 (1994)

Rettenberger, G., Fries, R., Engel, W., Scheit, K. H., Dolf, G., Hameister, H.: Establishment of a partially informative porcine somatic cell hybrid panel and assignment of the loci for transition protein 2 (TNP2) and protamine 1 (PRM1) to chromosome 3 and polyubiquitin (UBC) to chromosome 14. Genomics 21, 558-566 (1994)

Rickers, A., Rininsland, F., Osborne, L., Reiss, J.: Skipping of multiple CFTR exons is not a result of single exon omissions. Human Genetics 94, 311-313 (1994)

Rininsland, F., Reiss, J.: Microlesions and polymorphisms in the Duchenne/Becker muscular dystrophy gene. Human Genetics 94, 111-116 (1994)

Schlicker, M., Schnülle, V., Schneppel, L., Vorob'ev, V. I., Engel, W.: Disturbances of nuclear condensation in human spermatozoa: search for mutations in the genes for protamine 1, protamine 2 and transition protein 1. Human Reproduction 9, 2313-2317 (1994)

Schlote, D., Niesing, B., Rossak, M., Hummler, E., Beermann, F., Hansmann, I.: Homozygotic lethality and a complex malformation pattern is associated with expression of the transgenic "mos" in mouse line TG43. Medizinische Genetik 6, 145 (1994)

Schlüter, G., Wick, U.: An 87 bp deletion in exon 5 of the LDL receptor gene in a mother and her son with familial hypercholesterolemia. Clinical Genetics 45, 84-87 (1994)

Schnülle, V., Schlicker, M., Engel, W.: A (GA)_n repeat polymorphism in the human protamine 2 (PRM 2) gene. Human Molecular Genetics 3, 1445 (1994)

Schubert, S., Laccone, F., Lefterov, I., Nacheva, M., Hansmann, I.: Molecular mapping of a chromosome 20q-segment associated with seizures. Medizinische Genetik 6, 107, (1994)

Schubert, S., Laccone, F., Lefterov, I., Nacheva, M., Hansmann, I.: Towards positional cloning of the locus for benign neonatal epilepsy (EBN!) on chromosome 20. American Journal of Human Genetics 55, A 270 (1994).

Smith, C. L., Keith, T., Hansmann, I., Weissenbach, J., Asimakopoulos, F. A., Bowden, D., W., Deleuze, J. F., Dutton, E. R., Fasman, K. H., Green, T., Hadchouel, M., Hazan, J., Hilgartner, S., Kingsbury, D. K., Loder, B., Malafosse, A., Meunier-Rotival, M., Pearson, P. L., Siracusa, L. D., Steinlein, O., White, N., Williamson, C. M.: Report of the first international workshop on human chromosome 20 mapping 1993. Cytogenetics and Cell genetics 66, 78-82 (1994)

Thies, U.: Reply to Donna Wallerstein. Prenatal Diagnosis 4, 322-323 (1994)

Thies, U., Bockel, B., Bochdalofsky, V.: Chorea Huntington: Neue Erkenntnisse bei der präklinischen DNA-Diagnostik. Niedersächsisches Ärzteblatt 5, 45-46 (1994)

Von der Kammer, H., Löffler, C., Hanes, J., Klaudiny, J., Scheit, K. H., Hansmann, I.: The gene for the amyloid precursor-like protein APLP2 is assigned to human chromosome 11q23-q25. Genomics 10, 308-311 (1994)

Wunderle, V., Dibs, C., Fizames, C., Morisette, J., Hazan, J., Hansmann, I., Whitehouse, D., Vergnaud, G., Weissenbach, J.: The EUROGEM map of human chromosome 20. European Journal of Human Genetics 2, 242-243 (1994)

Zoll, B.: Neuere Möglichkeiten des Konduktorinnennachweises und der Pränataldiagnose von Hämophilie A und B. in: Psychosoziale Aspekte bei Hämophilie und HIV. Kurme, A., Klose, H. J., Beer, H.-J. (Hrsg.) Thieme Verlag Stuttgart, New York, 1994, S. 204-209 (1994)

Zoll, B., Knobloch, O.: Erfordernisse und Möglichkeiten genetischer Familienberatung bei Gerinnungsstörungen unter besonderer Berücksichtigung psychosozialer Aspekte pränataler Diagnostik und des Konduktorinnennachweises. in: Psychosoziale Aspekte bei Hämophilie und HIV. Kurme, A., Klose, H. J., Beer, H.-J. (Hrsg.) Thieme Verlag Stuttgart, New York, 1994, S. 210-217 (1994)

Zoll, B., Knobloch, O.: Anwendung neuer Strategien bei der Diagnostik in Familien mit Hämophilien. in: Psychosoziale Aspekte bei Hämophilie und HIV. Kurme, A., Klose, H. J., Beer, H. J. (Hrsg.) Thieme Verlag Stuttgart New York, 1994, S. 218-221 (1994)

Zühlke, C.: DNA-Diagnostik bei der Chorea Huntington. Ärzteblatt Rheinland-Pfalz 9, 273-274 (1994)

Zühlke, C., Thies, U., Braulke, I., Reis, A., Schirren, C.: Down syndrome and male fertility: PCR-derived fingerprinting, serological and andrological investigations. Clinical Genetics 46, 324-326 (1994)

Zühlke, C., Riess, O.: Gründung eines Konsortiums zur molekulargenetischen Diagnostik bei der Huntington Krankheit. Medizinische Genetik 4, 375 (1994)

Zühlke, C.: Tagungsbericht über das Symposium "Klinische und genetische Aspekte der Huntington- Krankheit und der Heredo-Ataxien" am 29.10. 1994 in Göttingen. Medizinische Genetik 4, 419-420 (1994)

1995

Diedrich, U., Lucius, J., Bittermann, H.-J., Schlösser, M., Eckert, B., Behnke, J., Pabst, B.: Loss of alleles in brain tumours: distribution and correlations with clinical course. Journal of Neurology 242, 707-711 (1995).

Diedrich, U., Lucius, J., Baron, E., Behnke, J.,Pabst, B., Zoll, B.: Distribution of epidermal growth factor receptor gene amplification in brain tumours and correlation to prognosis. Journal of Neurology 242, 683-688 (1995).

Engel, W.: Zukunftsperspektiven der Pränataldiagnostik. Amberger Symposion 17.-19.06.1994, S. 42-50.

Engel, W., Schmid, M.: Gibt es genetische Risiken der mikroassistierten Reproduktion? Fertilität 11, 214-228 (1995).

Engel, W., Schmid, M.: Kommentar zum Artikel von G. Bettendorf "Assistierte Fertilisation - ist eine Grenze erreicht oder bereits überschritten?" Der Frauenarzt 36, 1005-1009 (9/1995).

Hol, F.A., Hamel, B.C.J., Geurds, M.P.A., Hansmann, I., Nabben, F.A.E., Daniels, O., Mariman, E.C.M.: Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three generation family. Human Genetics 95, 687-690 (1995).

Jörgensen, G.: Inwieweit ist Sucht genetisch bedingt? Borsuye 26, 20-21 (1995).

Keith, T., Hansmann, I.: Report of the committee on the genetic constitution of chromosome 20. Human Gene Mapping 1994, a Compendium; Cuticchia A.J., Pearson P.L. (eds); Johns Hopkins University Press, Baltimore (1995).

Kim, Y., Adham, I. M., Haack, T., Kremling, H., Engel, W.: Molecular Cloning and Characterization of the Bovine and Porcine Outer Dense Fibers cDNA and Organization of the Bovine Gene. Biological Chemistry Hoppe Seyler 376, 431-435 (1995).

Knobloch, O., Schlösser, M., Diedrich, U., Kreuz, F.: Direkte DNA-Diagnostik einer Form der Spinozerebellären Ataxien jetzt möglich. Deutsches Ärzteblatt 92, A: 1102-1104; B: 821-823; C: 714-716 (1995).

Koehler, M.R., Neuhaus, D., Engel, W., Schartl, M., Schmid, M.: Evidence for an unusual ZW/ZW'/ZZ sex-chromosome system in Scardinius erythrophthalmus (Pisces, Cyprinidae), as detected by cytogenetic and H-Y antigen analyses. Cytogenetics and Cell Genetics 71, 356-362 (1995).

Kohlhase, J., Zoll, B.: Zur Genetik der geistigen Behinderung. Niedersächsisches Ärzteblatt 68, 12-15 (1995)

Kremling, H., Nayernia, K., Nieter, S., Bunkowski, S., Engel, W.: DNA-Protein binding studies in the 5´flanking region of rat proacrosin gene which is transcribed in diploid germ cells. Biological Chemistry Hoppe-Seyler 376, 187-193 (1995).

Laccone, F.: Williams-Beuren-Syndrom. Deutsches Ärzteblatt 92, A: 1382-1384; B: 1027-1029; C: 899-901 (1995).

Rauskolb, R., Engel, W.: Triple-Test: Problem oder Bereicherung der pränatalen Diagnostik. Zeitschrift f. Geburtshilfe und Neonatologie 199, 91 (1995).

Sancken, U., Bahner, D.: The effect of thermal instability of intact human chorionic gonadotropin (ihCG) on the application of its free ß-subunit (free ßhCG) as a serum marker in Down Syndrome screening. Prenatal Diagnosis 15, 731-738 (1995).

Seeman, P., Laccone, F., Reiss, J., Stoppe, G.: Absence of mutations in the apolipoprotein E (APOE) gene of patients with Alzheimer disease. Human Mutation 5, 103-104 (1995).

Schäfer, M., Nayernia, K., Engel, W., Schäfer, U.: Review. Translational Control in Spermatogenesis. Developmental Biology 172, 344-352 (1995).

Schloesser, M., Hofferbert, S., Bartz, U., Lutze, G., Lämmle, B., Engel, W.: The novel acceptor splice site mutation 11396 (GàA) in the factor XII gene causes a truncated transcript in cross-reacting material negative patients. Human Molecular Genetics 4, 1235-1237 (1995).

Schlüter, G., Engel, W.: The rat Prm3 gene is an intronless member of the protamine gene cluster and is expressed in haploid male germ cells. Cytogenetics and Cell Genetics 71, 352-355 (1995).

Wick, U., Witt, E., Engel, W.: Restriction fragment length polymorphisms at the apoprotein genes AI, CIII and B-100 and in the 5' flanking region of the insulin gene as possible markers of coronary heart disease. Clinical Genetics 47, 184-190 (1995).

Wiese, S., Murphy, D.B., Schlung, A., Burfeind, P., Schmundt, D., Schnülle, V., Mattei, M.-G., Thies, U.:The genes for human brain factor 1 and 2, members of the fork head gene family, are clustered on chromosome 14q. Biochimica et Biophysica Acta 1262, 105-112 (1995).

Zühlke, C., Knobloch, O., Wagner, S.: Allele distribution of a highly polymorphic repeat on chromosome 12 in patients with symptoms of chorea and ataxia. Journal of Medical Genetics 32, 577-578 (1995).

1996

Adham, I.M., Burkhardt-Göttges, E., Engel, W.: The Leydig insulin-like peptide. J. Anim. Breed. Genet. 113, 229-235 (1996)

Adham, I.M.,Tessmann, D., Soliman, K.A., Murphy, D., Kremling, H., Szpirer, C., Engel, W.: Cloning, expression, and chromosomal localization of the rat mitochondrial capsule selenoprotein gene (MCS): The reading frame does not contain potential UGA selenocysteine codons. DNA Cell Biol. 15, 159-166 (1996)

Adham, I.M., Kremling, H., Nieter, S., Zimmermann, S., Hummel, M., Schroeter, U., Engel, W.: The structures of the bovine and porcine proacrosin genes and their conservation among mammals. Biol. Chem. Hoppe-Seyler 377, 261-265 (1996)

Aho, H., Schwemmer, M., Tessmann, D., Murphy, D., Mattei, G., Engel, W., Adham, I.M.: Isolation, expression, and chromosomal localization of the human mitochondrial capsule selenoprotein gene (MCSP). Genomics 32, 184-190 (1996)

Bürk, K., Abele, M.,Fetter, M., Dichgans, J., Skalej, M., Laccone, F., Didierjean, O., Brice, A., Klockgether, T.: Autosomal dominant cerebellar ataxia type I Clinical features and MRI in families with SCA1, SCA2 and SCA3. Brain 119, 1497-1505 (1996)

Dreyling, M.H., Martinez-Climent, J. A., Zheng, M., Mao, J., Rowley, J. D., Bohlander, S. K.: The t (10; 11) (p13; q14) in the U937 cell line results in the fusion of the AF10 gene and CALM, encoding a new member of the AP-3-clathrin assembly protein family. Proc. Natl. Acad. Sci. USA 93, 4804-4809 (1996)

Eiben, B., Sancken, U.: Computer software programs and Down's syndrome risk calculations. The Lancet 347, 1553-1554 (1996)

Engel, W., Murphy, D., Schmid, M.: Are there genetic risks associated with microassisted reproduction? Hum. Reprod. 11, 2359-2370 (1996)

Fears, S., Vignon, C., Bohlander, S. K., Smith, S., Rowley, J. D., Nucifora, G.: Correlation between the ETV6/CBFA2 (TEL/AMLI) fusion gene and karyotypic abnormalities in children with B-Cell precursor acute Lymphoblastic Leukemia. Genes, Chromosomes & Cancer 17, 127-135 (1996)

Gu, S.-M., Orth, U., Veske, A., Enders, H., Klünder, K., Schlösser, M., Engel, W., Schwinger, E., Gal., A.: Five novel mutations in the L1CAM gene in families with X linked hydrocephalus. J. Med. Genet. 33, 103-106 (1996)

Guttenbach, M., Martinez-Exp¢sito, M. J., Engel, W., Schmid, M.: Interphase chromosome arrangement in Sertoli cells of adult mice. Biol. Reprod. 54, 980-986 (1996)

Hofferbert, S., Müller, J., Köstering, H., von Ohlen, W.-D., Schloesser, M.: A novel 5'-upstream mutation in the factor XII gene is associated with a Taql restriction site in an Alu repeat in factor XII-deficient patients. Hum. Genet. 97, 838-841 (1996)

Kim, B. D.-H., Moldwin, R. L., Vignon, C., Bohlander, S. K., Suto, Y., Giordano, L., Gupta, R., Fears, S., Nucifora, G., Rowley, J. D., Smith, S. D.: TEL-AML1 translocations with TEL and CDKN2 inactivation in acute lymphoblastic leukemia cell lines. Blood 88, 785-794 (1996)

Klockgether, T., Kramer, B., Lüdtke, R., Schöls, L., Laccone, F.: Repeat length and disease progression in spinocerebellar ataxia type 3. The Lancet 348, 830 (1996)

Koehler, M. R., Bosserhoff, A.-K., von Beust, G., Bauer, A., Blesch, A., Buettner, R., Schlegel, J., Bogdahn, U., Schmid, M.: Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32- q13.33 by fluorescence in situ hybridization (FISH). Genomics 35, 265-267 (1996)

Kohlhase, J., Schuh, R., Dowe, G., Kühnlein, R. P., Jäckle, H., Schroeder, B., Schulz-Schaeffer, W., Kretzschmar, H. A., Köhler, A., Müller, U., Raab-Vetter, M., Burkhardt, E., Engel, W., Stick , R.: Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt. Genomics 38, 291-298 (1996)

Korenke, G. C., Pouwel,s P. J. W., Frahm, J., Hunneman, D. H., Stoeckler, S., Krasemann, E., Jost, W., Hanefeld, F.: Arrested cerebral Adrenoleukodystrophy: a clinical and proton magnetic resonance spectroscopy study in three patients. Ann. Neurol. 40, 254-257(1996)

Korenke, Krasemann, E.W., Meier, V., Korenke, G. C., Hunneman, D. H., Hanefeld, F.: Identification of mutations in the ALD-gene of 20 families with adrenoleukodystrophy/ adrenomyeloneuropathy. Hum. Genet. 97, 194-197 (1996)

Kreuz, F. R: Attitudes of german persons at risk for Huntington's Disease toward predictive and prenatal testing. Genetic Counseling 7, 303-311 (1996)

Nayernia, K., Adham, I., Kremling, H., Reim, K., Schlicker, M., Schlüter, G., Engel, W.: Stage and developmental specific gene expression during mammalian spermatogenesis. Int. J. Dev. Biol. 40, 379-383 (1996)

Pauer, H.-U., Zoll, B., Köstering, H., Köhler, M., Schlösser, M.: Thromboemboliegefährdung und Mutation im Faktor V-Gen. Niedersächsisches Ärzteblatt 69, 33-35 (1996)

Schlüter, G.,Celik, A., Obata, R., Schlicker, M., Hofferbert, S., Schlung, A., Adham, I. M., Engel,, W.: Sequence analysis of the conserved protamine gene cluster shows that it contains a fourth expressed gene. Mol. Reprod. Dev. 43, 1-6 (1996)

Stegmaier, K., Takeuchi, S., Golub, T. R., Bohlander, S. K., Bartram, C. R., Koeffler, H. P., Gilliland, D. G.: Mutational analysis of the candidate tumor suppressor genes TEL and KIP1 in childhood acute lymphoblastic leukemia. Cancer Research 56, 1413-1417 (1996)

Stoffel, M., Le Beau, M. M., Espinosa III, R., Bohlander, S. K., Le Paslier, D., Cohen, D., Xiang, K. S., Cox, N. J., Fajans, S. S., Bell, C. I.: A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1 and a myeloid leukemia related gene. Proceedings of the National Academy of Sciences 93, 3937-3941 (1996)

Tanabe, S., Bohlander, S. K., Vignon, C. V., Espinosa III, R., Zhao, N., Strissel, P. L., Zeleznik-Le, N., Rowley, J. D.: AF10 is split by MLL and HEAB, a human analogue to a putative Caenorhabditis elegans ATP binding protein in an inv(10;11) (p12;q23q12). Blood 88, 3535-3545 (1996)

Vogt, P.H., Edelmann, A., Kirsch, S., Henegariu, O., Hirschmann, P., Kiesewetter, F., Köhn, F. M., Schill, W. B., Farah, S., Ramos, C., Hartmann, M., Hartschuh, W., Meschede, D., Behre, H. M., Castel, A., Nieschlag, E., Weidner, W., Gröne, H.-J., Jung, A., Engel, W., Haidl, G.: Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Human Molecular Genetics 5, 933-943 (1996)

Zimmermann, R., Reynolds, T. M., John, R., Spencer, K., Bartels, I., Coombes, E., Trevor, S.: Age-Independent indices in second-trimester serum screening for Down's Syndrome are useless. Prenatal Diagnosis, 16, 79-82 (1996)

Zühlke, C., Thies, U.: Chorea Huntington. Molekulargenetische Grundlagen, Mutationsnachweis und prädiktive Diagnostik. Nervenarzt 67, 25-35 (1996)

1997

Abele, M., Bürk, K., Andres, F., Topka, H., Laccone, F., Bösch, S., Brice, A., Cancel, G., Dichgans, J., Klockgether, T.: Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3. Brain 120, 2141-2148 (1997)

Adham, I. M., Nayernia, K., Engel, W.: Spermatozoa lacking acrosin protein show delayed fertilization. Molecular Reproduction and Development 46, 370-376 (1997)

Bartels, I., Franke, U., Braulke, I., Rauskolb, R., Raab-Vetter, M.: Normal outcome of a pregnancy with mosaicism for double trisomy in amniotic fluid cells. Prenatal Diagnosis 17, 877-878 (1997)

Bartels, I.: Serummarker zur Erkennung von fetalen Chromosomenstörungen. Archives of Gynecology and Obstetrics 260, 95-98 (1997)

Bürk, K., Fetter, M., Skalej, M., Laccone, F., Stevanin, G., Dichgans, J.,Klockgether, T.: Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia. Journal of Neurology, Neurosurgery & Psychiatry 62, 662-664 (1997)

Dreyling, M. H., Olopade, O. I., Bohlander, S. K.: Generation of small insert genomic FISH probes with high signal intensity suitable for deletion mapping. Cytogenetics and Cell Genetics 76, 202-205 (1997)

Emmerich, D., Orth, M., Zoll, B.: Genetische Aspekte der Koronaren Herzerkrankung. Niedersächsisches Ärzteblatt 70, 13-17 (1997)

Franke, Y.: Physical mapping of the Alagille syndrome chromosomal region 20p11.23-p12.1 and search for transcriptionally active sequences. B. I. F. Futura 12, 285-288 (1997)

Guttenbach, M., Engel, W., Schmid, M.: Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations. A review. Human Genetics 100, 1-21 (1997)

Guttenbach, M., Martinez-Exposito, M. J., Michelmann, H. W., Engel, W., Schmid, M.: Incidence of diploid and disomic sperm nuclei in 45 infertile men. Human Reproduction 12, 468-473 (1997)

Guttenbach, M., Michelmann, H. W., Hinney, B., Engel, W., Schmid, M.: Segregation of sex chromosomes into sperm nuclei in a man with 47,XXY Klinefelter's karyotype: a FISH analysis. Human Genetics 99, 474-477 (1997)

Koehler, M. R., von Beust, G., Engel, W., Schmid, M.: Assignment of the germ cell cyritestin gene 2 (CYRN2) to human chromosome 16q12.1 by fluorescence in situ hybridization to 5-azacytidine induced, partially decondensed chromosomes. Cytogenetics and Cell Genetics 77, 178-179 (1997)

Laccone, F., Schlösser, M.: A novel point mutation Met1IIe in the X25 gene responsible for Friedreich's Ataxia. Mutation Research, Mutation and Polymorphism, Report # 2. Online publication

Lange, R., Krause, W., Engel, W.: Analyses of meiotic chromosomes in testicular biopsies of infertile patients. Human Reproduction 12, 2154-2158 (1997)

Murphy, D. B., Seemann, S., Wiese, S., Kirschner, R., Grzeschik, K. H., Thies, U.: The human hepatocyte nuclear factor 3/fork head gene FKHL13: Genomic structure and pattern of expression. Genomics 40, 462-469 (1997)

Neesen, J., Koehler, M. R., Kirschner, R., Steinlein, C., Kreutzberger, J., Engel, W., Schmid, M.: Identification of dynein heavy chain genes expressed in human and mouse testis: chromosomal localization of an axonemal dynein gene. Gene 200,193-202 (1997)

Riess, O., Laccone, F., Gispert, S., Schöls, L., Zühlke, C., Menezes Vieira-Saecker, A. M., Herlt, S., Wessel, K., Epplen, J. T., Weber, B. H. F., Kreuz, F., Chahrokh-Zadeh, S., Meindl, A., Lunkes, A., Aguiar, J., Macek, M., Jr., Krebsova, A., Macek, M., Sen., Bürk, K.,Tinschert, S., Schreyer, I., Pulst, S. M., Auburger, G.: SCA2 trinucleotide expansion in German SCA patients. Neurogenetics 1, 59-64 (1997)

Riess, O., Schöls, L., Böttger, H., Nolte, D., Menezes Vieira-Saecker, A. M., Schimming, C., Kreuz, F., Macek, M., Jr., Krebsova, A., Macek, M., Sen., Klockgether, T., Zühlke, C., Laccone, F.: SCA6 is caused by moderate CAG expansion in the a_1A-voltage-dependent calcium channel gene. Human Molecular Genetics 6, 1289-1293 (1997)

Sato, Y., Bohlander, S. K., Kobayashi, H., Suto, Y., Davis, E. M., Le Beau, M. M., Rowley, J. D.: Identification of pericentric inversion 12, inv(12)(p13.1q11), by fluorescence in situ hybridization in a patient with acute myeloid leukemia (AML-M6). Cancer Genetics and Cytogenetics 97, 157-160 (1997)

Sato, Y., Bohlander, S. K., Kobayashi, H., Reshmi, S., Suto, Y., Davis, E. M., Espinosa III, R:, Hoopes, R., Montgomery, K., Kucherlapati, R. S., Le Beau, M. M., Rowley, J. D.: Heterogeneity in the breakpoints in balanced rearrangements involving band 12p13 in hematologic malignancies identified by fluorescence in situ hybridization: TEL (ETV6) is involved in only one half. Blood 90, 4886-4893 (1997)

Schlicker, M., Reim, K., Schlüter, G., Engel, W.: Specific binding of a 47-Kilodalton protein to the 3' untranslated region of rat transition protein 2 messenger ribonucleic acid. Biology of Reproduction 56, 697-706 (1997)

Schlösser, M., Zeerleder, S., Lutze, G., Halbmayer, W.-M., Hofferbert, S., Hinney, B., Koestering, H., Lämmle, B., Pindur, G., Thies, K., Köhler, M., Engel, W.: Mutations in the human factor XII gene. Blood 90, 3967-3977 (1997)

Schlösser, M., Vogelsang, S., Engel, W.: Mikrodeletionen im Y-Chromosom als Ursache männlicher Infertilität? Fertilität 13, 95-98 (1997)

Schlösser, M., Engel, W.: Mutationen im Faktor XII-Gen. aus: Molekulargenetik Hereditärer Hämostasedefekte, Hrsg. von F. H. Herrmann, 1996.

Suto, Y., Sato, Y., Smith, S. D., Rowley, J. D., Bohlander, S. K.: A t(6;12)(q23;p13) results in the fusion of ETV6 to a novel gene, STL, in a B-cell ALL cell line. Genes, Chromosomes and Cancer 18, 254-268 (1997)

Wiese, S., Emmerich, D., Schröder, B., Murphy, D. B., Grzeschik, K. H., Geurts van Kessel, A., Thies, U.: The novel human HNF-3/fork head-like 5 gene: chromosomal localization and expression pattern. DNA and Cell Biology 16, 165-171 (1997)

Zimmermann, S., Schöttler, P., Engel, W., Adham, I. M.: Mouse Leydig insulin-like (Ley-I-L) gene: Structure and expression during testis and ovary development. Molecular Reproduction and Development 47, 30-38 (1997)

1998

Adham, I. M., Kim, Y., Shamsadin, R., Heinlein, U. A. O., von Beust, G., Mattel, M.-G., Engel, W.: Molecular cloning, chromosomal localization, and expression analysis of CYRN1 and CYRN2, two human genes coding for Cyritestin, a sperm protein involved in Gamete interaction. DNA and Cell Biology 17, 161-168 (1998)

Adham, I. M., Schlösser, M., Engel, W.: Acrosin. In "Handbook of proteolytic enzymes"; Barrett, A. J., Rawlings, N. D., Woessner, J. F. (Eds.) Academic Press, London, pp. 90-93 (1998)

Bartels, I., Schlösser, M., Bartz, U. G., Pauer, H.-U.: Paternal origin of trisomy 21 following intracytoplasmic sperm injection (ICSI). Human Reproduction 13, 3345-3346 (1998)

Dreyling, M. H., Schrader, K., Fonatsch, C., Schlegelberger, B., Haase, D., Schoch, C., Ludwig, W.- D., Löffler, H., Büchner, T., Wörmann, B., Hiddemann, W., Bohlander, S. K.: MLL and CALM are fused to AF10 in morphologically distinct subsets of acute Leukemia with translocation t(10;11): Both rearrangements are associated with a poor prognosis. Blood 91, 4662-4667 (1998)

Engel, W., Schmid, M., Pauer, H.-U.: Genetik und mikroassistierte Reproduktion durch intrazytoplasmatische Spermieninjektion. Deutsches Ärzteblatt 95, C 1415 - C 1420 (1998)

Frank, S., Zoll, B.: Mouse HNF-3/fork head homolog-1-like gene: Structure, chromosomal location, and expression in adult and embryonic kidney. DNA and Cell Biology 17, 679-688 (1998)

Hinney, B., Guttenbach, M., Schmid, M., Engel, W., Michelmann, H. W.: Pregnancy after intracytoplasmic sperm injection with sperm from a man with a 47,XXY Klinefelter's karyotype. Fertility and Sterility 68, 718-720 (1997)

Karadima, G., Bugge, M., Nicolaidis, P., Vassilopoulos, D., Avramopoulos, D., Grigoriadou, M., Albrecht, B., Passarge, E., Annerén, G., Blennow, E., Clausen, N., Galla-Voumvouraki, A., Tsezou, A., Kitsiou-Tzeli, S., Hahnemann, J. M., Hertz, J. M., Houge, G., Kuklík, M., Macek, M., Lacombe, D., Miller, K., Moncla, A., Pajares, L. I., Patsalis, P. C., Prieur, M., Vekemans, M., von Beust, G., Brøndum-Nielsen, K., Petersen, M. B.: Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism. European Journal of Human Genetics 6, 432-438 (1998)

Klockgether, T., Skalej, M., Wedekind, D., Luft, A. R., Welte, D., Schulz, J. B., Abele, M., Bürk, K., Laccone, F., Brice, A., Dichgans, J.: Autosomal dominant cerebellar ataxia type I MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3. Brain 121, 1687-1693 (1998)

Klockgether, T., Lüdtke, R., Kramer, B., Abele, M., Bürk, K., Schöls, L., Riess, O., Laccone, F., Boesch, S., Lopes-Cendes, I., Brice, A., Inzelberg, R., Zilber, N., Dichgans, J.: The natural history of degenerative ataxia: a retrospective study in 466 patients. Brain 121, 589-600 (1998)

Koehler, M. R., Schmid, M., Neesen, J.: Chromosomal localization of the human cytoplasmic dynein heavy chain gene DNCH2 to 11q21àq22.1 Cytogenetics and Cell Genetics 82, 123-125 (1998)

Kohlhase, J., Wischermann, A., Reichenbach, H., Froster, U., Engel, W.: Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome. Nature Genetics 18, 81-83 (1998)

Leblhuber, F., Walli, J., Jellinger, K., Tilz, G. P., Widner, B., Laccone, F., Fuchs, D.: Activated immune systeme in patients with Huntington's disease. Clinical Chemistry and Laboratory Medicine 36, 747-750 (1998)

Moghadam, S., Engel, W., Bougoussa, M., Hennen, G., Igout, A., Sancken, U.: Maternal serum placental growth hormone and insulin like growth factor binding proteins 1 and 3 in pregnancies affected by fetal aneuploidy and other abnormalities: implications for prenatal diagnosis of trisomy 21. Fetal Diagnosis and Therapy 13, 291-297 (1998)

Neesen, J., Kreutzberger, J., Kirschner, R., Helmkampf, S., Engel, W.: Identification and characterization of human and murine dynein heavy chain genes. Andrologia 30, 173 (1998)

Neesen, J., Engel, W.: Die genetische Basis struktureller und funktioneller Spermiendefekte. Medizinische Genetik 10, 13-14 (1998)

Nicolaidis, P., von Beust, G., Bugge, M., Karadima, G., Vassilopoulos, D., Brøndum-Nielsen, K., Petersen, M. B.: Analysis of the origin of the extra chromosome in trisomy 8 in 4 cases of spontaneous abortions. Fetal Diagnosis and Therapy 13, 42-45 (1998)

Pauer, H.-U., Neesen, J., Hinney, B.: Factor V Leiden and its relevance in patients with recurrent abortions. American Journal of Obstetrics and Gynecology, 178, 629 (1998)

Pauer, H.-U., Hinney, B., Michelmann, H. W., Krasemann, E. W., Zoll, B., Engel, W.: Relevance of genetic counselling in couples prior to intracytoplasmic sperm injection. Human Reproduction 12, 1909-1912 (1997)

Reiss, J., Cohen, N., Dorche, C., Mandel, H., Mendel, R. R., Stallmeyer, B., Zabot, M.-T., Dierks, T.: Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency. Nature Genetics 20, 51-53 (1998)

Reiss, J., Christensen, E., Kurlemann, G., Zabot, M.-T., Dorche, C.,: Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A. Human Genetics 103, 639-644 (1998)

Sancken, U., Rempen, A.: Die Bedeutung des Schwangerschaftsalters bei der individuellen Risikoberechnung für ein fetales Down-Syndrom in der sogenannten Triple-Diagnostik. Geburtshilfe und Frauenheilkunde 58, 219-224 (1998)

Schmidt, T., Landwehrmeyer, B., Schmitt, I., Trottier, Y., Auburger, G., Laccone, F., Klockgether, T., Völpel, M., Epplen, J. T., Schöls, L., Riess, O.: An isoform of Ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients. Brain Pathology 8, 669-679 (1998)

Shalata, A., Mandel, H., Reiss, J., Szargel, R., Cohen-Akenine, A., Dorche, C., Zabot, M.-T., van Gennip, A., Abeling, N., Berant, M., Cohen, N.: Localization of a gene for molybdenum cofactor deficiency, on the short arm of chromosome 6, by homozygosity mapping. American Journal of Human Genetics 63, 148-154 (1998)

Thies, U., Bartels, I., von Beust, G., Bink, K., Hansmann, I., Rehder, H., Suren, A., Zoll, B.: Prenatal diagnosis and fetopathological findings in a fetus with ring chromosome 18. Fetal Diagnosis and Therapy 13, 315-320 (1998)

Von Beust, G., Bartmus, D., Bartels, I.: Catch 22 - microdeletion 22q11 screening in patients with congenital heart defects. Genetic Counseling 9, 223-227 (1998)

Zimmermann, S., Schwärzler, A., Buth, S., Engel, W., Adham, I. M.: Transcription of the Leydig Insulin-like gene is mediated by steroidogenic factor-1. Molecular Endocrinology 12, 706-713 (1998)

Zühlke, C., Laccone, F., Cossée, M., Kohlschütter, A., Koenig, M., Schwinger, E.: Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestor. Human Genetics 103, 102-105 (1998)

1999