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Human Genetics|January 25, 1979
Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11)J P Fryns, P Casaer, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 31, 2006
Attitudes towards carrier testing in minors: a systematic reviewP Borry, J P Fryns, P Schotsmans, et al.Clinical Genetics|October 1, 1995
The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in 12 childrenA Swillen, N Glorieux, M Peeters, et al.Clinical Genetics|September 1, 1993
Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23J P Fryns, P Strømme, H van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Duplication in the long arm of the X-chromosome associated with spastic paraparesis and premature menopauseA Kleczkowska, J P Fryns, H Van den BergheAnnales De Genetique|January 1, 1993
A distinct multiple congenital anomalies syndrome associated with distal 5q deletion (q35.1qter)A Kleczkowska, J P Fryns, H van den BergheHuman Genetics|October 1, 1979
Down's syndrome in brother and sister without evident trisomy 21C Parloir, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1990
High incidence of mental retardation in Turner syndrome patients with ring chromosome X formationJ P Fryns, A Kleczkowska, H Van Den BergheJournal of Medical Genetics|August 1, 1989
Hypohidrotic ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosumJ P Fryns, K Chrzanowska, H Van den BergheAnnales De Genetique|January 1, 1995
Renal agenesis and trisomy 22: case report and reviewG J Van Buggenhout, J Verbruggen, J P FrynsPageof 90