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American Journal of Medical Genetics|January 1, 1994
Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome?J P Fryns, E Smeets, P Thiry, et al.Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Duplication of the VHL and IRAK2 genes in a patient with mental retardation/multiple congenital anomalies, epilepsy and ectomorphic habitusE Chabchoub, G Michils, J R Vermeesch, et al.American Journal of Medical Genetics|December 1, 1990
Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1)J P Fryns, A Kleczkowska, E Smeets, et al.American Journal of Medical Genetics|April 1, 1989
Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: a variant example of the Lenz-Majewski syndromeK H Chrzanowska, J P Fryns, M Krajewska-Walasek, et al.Journal of Medical Genetics|January 1, 1996
Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35)X X Gu, R Decorte, P Marynen, et al.Cytogenetics and Cell Genetics|September 8, 1998
Physical mapping of the t(12;22) translocation breakpoints in a family with a complex type of 3/3'/4 synpolydactylyP Debeer, E F Schoenmakers, R Thoelen, et al.Annales De Genetique|January 1, 1986
Acrocentric/18p translocation in two mentally retarded males. Delineation of the adult phenotypeJ P Fryns, A Kleczkowska, L Vinken, et al.Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Marden-Walker syndrome: case report, nosologic discussion and aspects of counselingL Garavelli, A Donadio, G Banchini, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Macrocephaly and mental retardation. The unique association with short stature, spastic paraplegia and CNS malformationsP Volcke, D Soekarman, P Vandenbussche, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1995
FG syndrome: the trias mental retardation, hypotonia and constipation reviewedA M Zwamborn-Hanssen, C T Schrander-Stumpel, E Smeets, et al.Pageof 89