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Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Miller postaxial acrofacial dysostosis. The phenotypic changes with ageK Chrzanowska, J P FrynsClinical Genetics|July 1, 1984
Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother. Another variant example of the KBG syndrome?J P Fryns, M HaspeslaghGenetic Counseling (Geneva, Switzerland)|January 22, 2005
Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndromeA Vogels, J P FrynsGenetic Counseling (Geneva, Switzerland)|July 16, 2008
Prenatal diagnosis of trisomy 21: registration results from a single genetic centerI Witters, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1990
Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effectP Petit, J P FrynsAmerican Journal of Medical Genetics|January 8, 1999
Syndrome of facial, oral, and digital anomalies due to 7q21.2-->q22.1 duplicationT Lukusa, J P FrynsGenetic Counseling (Geneva, Switzerland)|August 2, 2002
The velocardiofacial syndrome: a reviewA Vogels, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1997
Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosomeP Petit, J P FrynsPageof 89