Showing results (191-200 of 899) with videos related to
Sort By:
Pageof 90
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333))A Vogels, J Haegeman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Nager acrofacial dysostosis and preaxial polydactyly: a further example with lethal outcomeP Petit, P Moerman, 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 90