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American Journal of Medical Genetics|September 1, 1991
Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophyJ R Lupski, C A Garcia, H Y Zoghbi, et al.American Journal of Medical Genetics|October 1, 1991
Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patientsJ Hamabe, Y Fukushima, N Harada, et al.American Journal of Medical Genetics|March 15, 1991
DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the ChineseB W Soong, T F Tsai, C H Su, et al.American Journal of Medical Genetics|January 1, 1991
Autosomal recessive inheritance of vasopressin-resistant diabetes insipidusJ M Langley, J W Balfe, T Selander, et al.American Journal of Medical Genetics|September 15, 1991
Linkage of an Alzheimer disease susceptibility locus to markers on human chromosome 21L L Heston, H T Orr, S S Rich, et al.American Journal of Medical Genetics|March 1, 1990
DNA polymerase alpha defect in the N syndromeK M Floy, R O Hess, L F MeisnerAmerican Journal of Medical Genetics|December 1, 1990
Low molecular weight urinary peptides in ceroid-lipofuscinoses: potential biochemical markers for the juvenile subtypeG U LaBadie, R K PullarkatAmerican Journal of Medical Genetics|December 1, 1991
Analysis of neocortex in three males with the fragile X syndromeV J Hinton, W T Brown, K Wisniewski, et al.American Journal of Medical Genetics|September 15, 1991
Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutationsG Filippi, A Arslanian, F Dagna-Bricarelli, et al.American Journal of Medical Genetics|September 15, 1991
Hepatic dysfunction in Alström diseaseM B Connolly, J E Jan, R M Couch, et al.Pageof 854