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American Journal of Medical Genetics|July 15, 1994
Personality profile in adult female fragile X carriers: assessed with the Minnesota Multiphasic Personality Profile (MMPI)J Steyaert, M Decruyenaere, M Borghgraef, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Hyperacusis in Williams syndrome: a sample survey studyJ Van Borsel, L M Curfs, J P FrynsHuman Genetics|January 25, 1979
Partial duplication of the short arm of chromosome 9 (p13 leads to p22) in a child with typical 9p trisomy phenotypeJ P Fryns, P Casaer, H Van den BergheClinical Genetics|May 1, 1990
The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriersM Borghgraef, J P Fryns, H van den BergheJournal of Medical Genetics|August 1, 1989
Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?E Legius, J P Fryns, H Van den BergheHuman Genetics|July 18, 1979
Partial trisomy 17q. Karyotype: 46,XY,der(21),t(17;21)(q22;p13)J P Fryns, C Parloir, H Van den BergheHuman Genetics|April 1, 1987
Pericentric inversions in man: personal experience and review of the literatureA Kleczkowska, J P Fryns, H Van den BergheJournal De Genetique Humaine|January 1, 1987
[An excess of mental retardation and/or congenital malformations in carriers of reciprocal translocations. A difficult and delicate problem in genetic counseling]J P Fryns, A Kleczkowska, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Opitz-C syndrome: on the nosology of mental retardation and trigonocephalyC Schaap, C T Schrander-Stumpel, J P FrynsAmerican Journal of Medical Genetics|February 17, 2001
Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complicationsA Swillen, A Vogels, K Devriendt, et al.Pageof 89