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Prenatal Diagnosis|May 23, 2000
Diaphragmatic hernia as the first echographic sign in Apert syndromeI Witters, K Devriendt, P Moerman, et al.Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Duplication of the VHL and IRAK2 genes in a patient with mental retardation/multiple congenital anomalies, epilepsy and ectomorphic habitusE Chabchoub, G Michils, J R Vermeesch, et al.Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndromeN Rommel, G Vantrappen, A Swillen, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18pJ P Fryns, A Kleczkowska, K Devriendt, et al.Acta Oto-Rhino-Laryngologica Belgica|July 3, 2003
Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestationsG Vantrappen, N Rommel, A Swillen, et al.Neuropsychologia|October 20, 2006
Mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.Journal of Intellectual Disability Research : JIDR|September 12, 2007
Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an updateB De Smedt, K Devriendt, J-P Fryns, et al.Clinical Dysmorphology|May 29, 2000
Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphismK Devriendt, K Keymolen, L Roelen, et al.Human Genetics|June 1, 1997
Interstitial telomeric sequences at the junction site of a jumping translocationJ R Vermeesch, P Petit, F Speleman, et al.Prenatal Diagnosis|March 4, 1998
Prenatal diagnosis of a terminal short arm deletion of chromosome 8 in a fetus with an atrioventricular septal defectK Devriendt, D Van Schoubroeck, B Eyskens, et al.Pageof 90