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Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The fetal akinesia deformation sequence. A fetopathological approachP Moerman, J P FrynsJournal De Genetique Humaine|September 1, 1985
[Lethal skeletal dysplasias: delineation of a new distinct entity with spondylocostal dysostosis, multiple internal abnormalities and Dandy-Walker cyst]J P Fryns, P MoermanAnnales De Genetique|January 1, 1996
Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patientJ P Fryns, G HendrickxGenetic Counseling (Geneva, Switzerland)|July 28, 1999
Early development (5 to 48 months) in Williams syndrome. A study of 14 childrenL Plissart, J P FrynsAmerican Journal of Medical Genetics|June 14, 1996
Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her childP Moerman, J P FrynsGenetic 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 FrynsPageof 90