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American Journal of Medical Genetics|July 9, 1999
Down syndrome in a population of elderly mentally retarded patients: genetic-diagnostic survey and implications for medical careG J Van Buggenhout, J C Trommelen, A Schoenmaker, et al.Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Progeroid syndrome with facial teleangiectatic erythema, posterior subcapsular cataracts, calcification of basal ganglia and atrium septum defect type 2J P Fryns, M Dumoulin, G HensClinical Genetics|April 1, 1984
Severe limb malformations in 4p deletionM Haspeslagh, J P Fryns, P MoermanGenetic Counseling (Geneva, Switzerland)|January 1, 1991
X-linked mental retardation with Marfanoid habitus: a changing phenotype with age?J P Fryns, H Van Den BergheGenetic Counseling (Geneva, Switzerland)|November 11, 2008
Skeletal dysplasias: 38 prenatal casesI Witters, Ph Moerman, J P FrynsHuman Genetics|October 1, 1990
Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologueD Wöhrle, J P Fryns, P SteinbachHuman Genetics|June 19, 1979
Congenital scalp defects associated with postaxial polydactylyJ P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|May 3, 2001
Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic featuresE Smeets, L Vandenbossche, J P FrynsAnnales De Genetique|January 1, 1984
De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boyJ P Fryns, A Kleczkowska, H KenisEuropean Journal of Pediatrics|June 28, 1979
Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation--a new syndrome?J P Fryns, H Van den BerghePageof 90