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Clinical Genetics|April 19, 2003
Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual impairmentC Windpassinger, E Petek, K Wagner, et al.American Journal of Medical Genetics|June 26, 2001
Candidate region for Gilles de la Tourette syndrome at 7q31P M Kroisel, E Petek, W Emberger, et al.Clinical Dysmorphology|April 20, 2001
Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)E Petek, G Köstl, L Rauter, et al.Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Characterisation of a 19-year-old "long-term survivor" with Edwards syndromeE Petek, B Pertl, M Tschernigg, et al.Cancer Genetics and Cytogenetics|August 25, 2001
Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11)W Emberger, A Behmel, M Tschernigg, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Localization of genes and anonymous DNA probes on the short arm of chromosome 7K Wagner, P M Kroisel, W RosenkranzCytogenetic and Genome Research|September 16, 2006
Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech developmentT Schwarzbraun, R Ullmann, M Schubert, et al.Genomics|November 1, 1990
Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genesK Wagner, P M Kroisel, W RosenkranzClinical 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.American Journal of Human Genetics|March 20, 2001
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndromeE Petek, C Windpassinger, J B Vincent, et al.Pageof 157