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Clinical Genetics|October 1, 1986
A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patientsJ P Fryns, A Kleczkowska, A Dereymaeker, et al.Clinical Genetics|November 15, 2002
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)P Debeer, R Mols, C Huysmans, 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.American Journal of Human Genetics|January 1, 1995
Two new cases of FMR1 deletion associated with mental impairmentM Hirst, P Grewal, A Flannery, et al.Clinical Genetics|December 1, 1985
Mental retardation with pterygia, shortness and distinct facial appearance. A new MCA/MR syndromeM Haspeslagh, J P Fryns, A de Mûelenaere, et al.Prenatal Diagnosis|May 10, 2002
Prenatal findings in a monozygotic twin pregnancy with Costello syndromeT Van den Bosch, D Van Schoubroeck, J P Fryns, et al.European Journal of Human Genetics : EJHG|December 18, 2003
Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in FlandersAnnick Vogels, Jenneke Van Den Ende, Kathelijne Keymolen, et al.Journal of Medical Genetics|November 2, 1999
Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?U Moog, P Maroteaux, C T Schrander-Stumpel, et al.Clinical Dysmorphology|October 23, 2001
Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factorT J de Ravel, E Legius, H Brems, et al.Journal of Medical Genetics|July 1, 1995
Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSASJ C Ruiz, H Cuppens, E Legius, et al.Pageof 89