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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 HensGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 geneJ P Fryns, M D'Hooghe, K DevriendtGenetic 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 BergheAnnales De Genetique|January 1, 1979
Possible excess of mental handicap and congenital malformations in autosomal reciprocal translocationsJ P Fryns, H van den BergheAmerican Journal of Medical Genetics|January 1, 1988
Acrofacial dysostosis with postaxial limb deficiencyJ P Fryns, H Van den BergheClinical Genetics|October 1, 1986
An asymmetric type of chondrodysplasia in an adult male. Another example of postzygotic mutation for an autosomal dominant gene?J P Fryns, H van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1997
On the nosology of the craniodigital syndromes: report of a family and review of the literatureD Soekarman, P Volcke, J P FrynsPageof 89