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Genetic Counseling (Geneva, Switzerland)|January 1, 1991
X-linked mental retardation with Marfanoid habitus: a changing phenotype with age?J P Fryns, H Van Den BergheHuman Genetics|June 19, 1979
Congenital scalp defects associated with postaxial polydactylyJ P Fryns, H Van den BergheEuropean 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 BergheHuman Genetics|March 12, 1979
Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the motherJ P Fryns, H Van den BergheAmerican Journal of Medical Genetics|May 1, 1988
Inactivation pattern of the fragile X in heterozygous carriersJ P Fryns, H Van den BergheEuropean Journal of Pediatrics|January 1, 1988
Facial paralysis at the age of 2 months as a first clinical sign of van Buchem disease (endosteal hyperostosis)J P Fryns, H Van den BergheAmerican Journal of Medical Genetics|May 1, 1988
The concurrence of Klinefelter syndrome and fragile X syndromeJ 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 BerghePageof 124