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Clinical Dysmorphology|February 2, 2002
Monosomy 1p36--a recently delineated, clinically recognizable syndromeM Zenker, O Rittinger, K P Grosse, et al.Annals of Hematology|May 1, 1996
LW/SO cell line: a tool for studying the phenotypical characterization and commitment of hematopoietic stem cellsS Oez, U Trautmann, M Smetak, et al.Human Genetics|September 1, 1992
Multiple minute marker chromosomes derived from Y identified by FISH in an intersexual infantL Diekmann, K Palm, R A Pfeiffer, et al.American Journal of Medical Genetics|August 26, 1998
Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic archA Rauch, M Hofbeck, G Leipold, et al.Cancer Genetics and Cytogenetics|February 13, 2001
Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasiasI Verdorfer, L Brecevic, W Saul, et al.Journal of Medical Genetics|December 14, 2004
Molecular karyotyping using an SNP array for genomewide genotypingA Rauch, F Rüschendorf, J Huang, et al.American Journal of Medical Genetics|March 17, 2001
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlationA Rauch, S Schellmoser, C Kraus, et al.Prenatal Diagnosis|December 17, 1998
Further observations of true mosaic trisomy 17 ascertained in amniotic fluid cell culturesM Djalali, G Barbi, J Mueller-Navia, et al.Prenatal Diagnosis|February 19, 1998
True fetal mosaicism of an isochromosome of the long arm of a chromosome 20: the dilemma persistsR A Pfeiffer, R Ulmer, A Rauch, et al.Leukemia|March 1, 1995
Therapy with OKT3 monoclonal antibody in refractory T cell acute lymphoblastic leukemia induces interleukin-2 responsivenessM Gramatzki, R Burger, G Strobel, et al.Pageof 5