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Genetic Counseling (Geneva, Switzerland)|May 3, 2003
Pre-academic and early academic achievement in children with velocardiofacial syndrome (del22q11.2) of borderline or normal intelligenceB De Smedt, A Swillen, P Ghesquière, et al.
Human Reproduction (Oxford, England)|October 9, 2004
Preimplantation genetic diagnosis for an insertional translocation carrierC Melotte, S Debrock, T D'Hooghe, et al.
American Journal of Medical Genetics|August 15, 1993
Adaptive behavior in the fragile X syndrome: profile and developmentA M Wiegers, L M Curfs, E L Vermeer, et al.
Clinical Genetics|April 1, 1988
Mental retardation, macrocephaly, short stature and craniofacial dysmorphism in three sisters. A new entity among the mental retardation-macrocephaly syndromes?J P Fryns, A M Dereymaeker, J Haegeman, et al.
Human Genetics|April 17, 1979
Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21)J P Fryns, N Logghe, M Van Eygen, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Fragile-X syndrome and autism: a prevalent association or a misinterpreted connection?B Maes, J P Fryns, M Van Walleghem, et al.
American Journal of Medical Genetics|April 1, 1994
Cognitive functioning and information processing of adult mentally retarded men with fragile-X syndromeB Maes, J P Fryns, M Van Walleghem, et al.
Human Genetics|January 1, 1985
9p Trisomy/18p distal monosomy and multiple cutaneous leiomyomata. Another specific chromosomal site (18pter) in dominantly inherited multiple tumors?J P Fryns, M Haspeslagh, A de Mûelenaere, et al.
American Journal of Medical Genetics|March 15, 1991
Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneityC Schrander-Stumpel, J P Fryns, F A Beemer, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorderT Lukusa, J R Vermeesch, M Holvoet, et al.
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