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Annales De Genetique|January 1, 1987
Distinct dysmorphic syndrome in a child with inverted distal 5q duplicationJ P Fryns, A Kleczkowska, M Borghgraef, et al.Journal of Mental Deficiency Research|June 1, 1990
The 49,XXXXY syndrome: clinical and psychological findings in five patientsL M Curfs, G Schreppers-Tijdink, A Wiegers, et al.Clinical Genetics|December 1, 1989
Strengths and weaknesses in the cognitive profile of fra(X) patientsL M Curfs, M Borghgraef, A Wiegers, et al.Clinical Genetics|January 1, 1992
Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entityC Grubben, P de Cock, M Borghgraef, et al.Clinical Genetics|December 1, 1991
Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndromeL M Curfs, A M Wiegers, J R Sommers, et al.American Journal of Medical Genetics|April 1, 1992
MASA syndrome: delineation of the clinical spectrum at prepubertal ageJ P Fryns, C Schrander-Stumpel, C De Die-Smulders, et al.Journal of Intellectual Disability Research : JIDR|February 25, 1999
Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studiesD Clarke, H Boer, T Webb, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Terminal deletion of long arm of chromosome 4: patient report and literature reviewL J Evers, C T Schrander-Stumpel, J J Engelen, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
The Prader-Willi syndrome: a self supporting program for children, youngsters and adultsM J Descheemaeker, A Swillen, L Plissart, et al.Journal of Intellectual Disability Research : JIDR|February 20, 2002
Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrumM J Descheemaeker, A Vogels, V Govers, et al.Pageof 4