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Clinical Genetics|December 8, 1998
Isolation of a 370 kb YAC fragment spanning a translocation breakpoint at 3p14.1 associated with holoprosencephalyE Petek, P M Kroisel, K WagnerAmerican Journal of Medical Genetics|August 3, 2001
Phenotype of five patients with Greig syndrome and microdeletion of 7p13P M Kroisel, E Petek, K WagnerGenetic Counseling (Geneva, Switzerland)|May 23, 2002
Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical regionM Tschernigg, E Petek, K Wagner, et al.Human Immunology|October 4, 2015
HLA-frequencies of Austrian umbilical cord blood samplesS Nerstheimer, P Tauscher, E Petek, et al.Cytogenetic and Genome Research|November 20, 2002
Chromosomal localization and genomic organization of the human Linker for Activation of T cells (LAT) geneC Windpassinger, P M Kroisel, K Wagner, et al.Clinical Dysmorphology|January 29, 2000
Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISHE Petek, G Köstl, I Mutz, et al.American Journal of Medical Genetics|December 26, 2001
Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndromeW Emberger, E Petek, P M Kroisel, et al.Clinical Genetics|March 18, 2008
Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the myelin transcription factor 1 gene (MYT1)T Kroepfl, E Petek, T Schwarzbraun, et al.Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13)M Tschernigg, E Petek, A Leonhardtsberger, et al.American Journal of Medical Genetics|May 20, 1999
Mosaicism in a fragile X male including a de novo deletion in the FMR1 geneE Petek, P M Kroisel, M Schuster, et al.Pageof 3