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American Journal of Medical Genetics|April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?G S Fisch, L R Shapiro, R Simensen, et al.Journal of Medical Genetics|December 1, 1991
Genotype prediction in the fragile X syndromeM C Hirst, Y Nakahori, S J Knight, et al.Clinical Genetics|September 1, 1996
Deletion of the long arm of chromosome 6: two new patients and literature reviewL J Evers, C T Schrander-Stumpel, J J Engelen, et al.Human Molecular Genetics|May 18, 2000
Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 geneM Veugelers, B D Cat, S Y Muyldermans, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Fountain syndrome: further delineation of the clinical syndrome and follow-up dataG J Van Buggenhout, C M Van Ravenswaaij-Arts, W O Renier, et al.Clinical Genetics|October 30, 2009
Novel PORCN mutations in focal dermal hypoplasiaG Froyen, K Govaerts, H Van Esch, et al.Human Molecular Genetics|April 1, 1994
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndromeH Meijer, E de Graaff, D M Merckx, et al.American Journal of Human Genetics|March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1K Devriendt, G Matthijs, R Van Dael, et al.Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Strong variable clinical presentation in 3 patients with 7q terminal deletionS G Frints, C T Schrander-Stumpel, E F Schoenmakers, et al.American Journal of Medical Genetics|July 9, 1999
Down syndrome in a population of elderly mentally retarded patients: genetic-diagnostic survey and implications for medical careG J Van Buggenhout, J C Trommelen, A Schoenmaker, et al.Pageof 89