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Annales De Genetique|January 1, 1997
Multiple (up to seven) different accessory small marker chromosomes: prenatal diagnosis and follow-upR Ulmer, R A Pfeiffer, E Wiest, et al.Journal of Medical Genetics|April 1, 1993
Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic featuresU Trautmann, R A Pfeiffer, U Seufert-Satomi, et al.Clinical Genetics|May 1, 1997
Brachydactyly in a child with duplication-deficiency subsequent to t(15;20)(q25.2;p12.2)mat. Candidate regions on one or both chromosomes?R A Pfeiffer, C Kändler, E Sieber, et al.Cancer Genetics and Cytogenetics|February 1, 1994
Tetrasomy 8 as a clonal anomaly in myeloid neoplasiasU Trautmann, M Gramatzki, M Krauss, et al.Clinical Genetics|April 1, 1997
Prenatal detection of double aneuploidy trisomy 10/monosomy X in a liveborn twin with exclusively monosomy X in bloodG Mielke, H Enders, R Goelz, et al.Prenatal Diagnosis|December 13, 2000
Prenatal diagnosis of heterokaryotypic mosaic twins discordant for fetal sexO Schmid, U Trautmann, H Ashour, et al.Clinical Genetics|August 1, 1992
A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)A Rauch, R A Pfeiffer, U Trautmann, et al.European Journal of Human Genetics : EJHG|April 26, 2000
FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primatesZ Shan, B Zabel, U Trautmann, et al.American Journal of Medical Genetics|February 5, 1998
Monozygotic twins concordant for Cayler syndromeA Rauch, M Hofbeck, S Bähring, et al.Leukemia & Lymphoma|April 1, 1995
Determination by interphase-FISH of the clonality of aberrant karyotypes in human hematopoietic neoplasiasE Gebhart, T Liehr, P Harrer, et al.Pageof 5