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Journal De Genetique Humaine|October 1, 1982
Small accessory chromosomes (SAC) and their genotype--phenotype correlationJ P Fryns, A Kleczkowska, H Van den Berghe
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: a distinct MCA/MR syndrome?C de Die-Smulders, H Vles, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Cenani-Lenz syndrome in father and daughterL De Smet, P De Beer, J P Fryns
American Journal of Medical Genetics|August 9, 1996
Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 geneJ Steyaert, M Borghgraef, E Legius, et al.
Human Genetics|May 10, 1977
The Coffin syndromeJ P Fryns, L Vinken, H Van den Berghe
European Journal of Pediatrics|November 4, 1977
Congenital scalp defect with distal limb reduction anomaliesJ P Fryns, L Corbeel, H Van den Berghe
American Journal of Medical Genetics|May 1, 1986
Distal deletion of the long arm of chromosome 6: a specific phenotype?J P Fryns, W Bettens, H Van den Berghe
Clinical Genetics|April 1, 1986
Gonadoblastoma and Y-chromosome fluorescenceT Lukusa, J P Fryns, H van den Berghe
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
The role of the Y-chromosome in sex determinationT Lukusa, J P Fryns, H van der Berghe
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