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Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotypeM Mach, C Windpassinger, K Wagner, et al.Prenatal Diagnosis|March 31, 2000
Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformationE Petek, K Wagner, H Steiner, et al.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.Genomics|November 15, 2001
Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31J Cheung, E Petek, K Nakabayashi, 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.QJM : Monthly Journal of the Association of Physicians|February 21, 2014
Multidisciplinary treatment of desmoid tumours in Gardner's syndrome due to a large interstitial deletion of chromosome 5qM Casper, E Petek, W Henn, et al.Brain : a Journal of Neurology|July 25, 2000
Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic studyM Auer-Grumbach, W N Löscher, K Wagner, et al.Pageof 3