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Journal of Medical Genetics|March 1, 1996
Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndromeK Devriendt, L D'Espallier, J P FrynsAmerican Journal of Medical Genetics|March 1, 1996
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?K Devriendt, E Legius, J P FrynsGenetic Counseling (Geneva, Switzerland)|October 28, 2003
The XYY syndrome: a follow-up study on 38 boysM Geerts, J Steyaert, J P FrynsClinical Genetics|October 1, 1994
The KBG syndrome: follow-up data on three affected brothersD Soekarman, P Volcke, J P FrynsAnnales De Genetique|January 1, 1980
Silver staining of the supernumerary chromosome in the cat-eye syndromeP Petit, S Godart, J P FrynsHuman 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 BergheClinical Genetics|April 1, 1997
Vocal cord paralysis and cystic kidney disease in Hajdu-Cheney syndromeJ P Fryns, C Stinckens, L FeenstraGenetic Counseling (Geneva, Switzerland)|November 2, 2005
A follow-up study on 12 prenatally diagnosed boys with Klinefelter syndromeG Meeus, J Steyaert, J P FrynsEuropean 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 BerghePageof 89