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Human Genetics|February 16, 1978
Partial trisomy for the long arm of chromosome 3 [3(q21 to qter)+] in a newborn with minor physical stigmataJ P Fryns, M van Eygen, N Logghe, et al.
Human Genetics|October 31, 1978
Partial trisomy 18q in a newborn with typical 18 trisomy phenotypeJ P Fryns, F Detavernier, A van Fleteren, et al.
Clinical Genetics|March 1, 1986
Genetic control over fragile X chromosome expressionF Hecht, J P Fryns, R F Vlietinck, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Terminal 6q25.3 deletion and abnormal behaviourT Lukusa, D Willekens, N Lukusa, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 genesA O Caglayan, S Lechno, H Gumus, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The lethal multiple pterygium syndrome: a nosological approachC E de Die-Smulders, C T Schrander-Stumpel, J P Fryns
Human Genetics|November 1, 1990
Selective advantage of fra (X) heterozygotesF Vogel, W E Crusio, C Kovac, et al.
Journal of Intellectual Disability Research : JIDR|June 1, 1995
Personality profiles of youngsters with Prader-Willi syndrome and youngsters attending regular schoolsL M Curfs, V Hoondert, C F van Lieshout, et al.
Annales De Genetique|January 1, 1980
Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthoodJ P Fryns, A de Muelenaere, J Pedersen, et al.
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