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Hormone Research|July 15, 2000
Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinismJ C Fournet, C Mayaud, P de Lonlay, et al.Cell|October 18, 1991
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndromeJ Pelletier, W Bruening, C E Kashtan, et al.Human Genetics|May 1, 1992
Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD)B Müller, C Dechant, G Meng, et al.Annales De Genetique|January 1, 1997
Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patientsT Bienvenu, M Adjiman, N Thiounn, et al.Nucleic Acids Research|February 25, 1983
Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22)A de la Chapelle, G Lenoir, J Boué, et al.Neuromuscular Disorders : NMD|May 5, 1998
Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenonD Annane, M Fiorelli, B Mazoyer, et al.Genomics|November 1, 1989
CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridiaW A Bickmore, D J Porteous, S Christie, et al.American Journal of Human Genetics|June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseC Jeanpierre, E Denamur, I Henry, et al.American Journal of Human Genetics|May 1, 1982
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridizationC Junien, D Weil, J C Myers, et al.Cell|August 26, 1994
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophyS L Roberds, F Leturcq, V Allamand, et al.Pageof 24