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Human Genetics|August 2, 2001
Glycerol kinase deficiency: evidence for complexity in a single gene disorderK M Dipple, Y H Zhang, B L Huang, et al.Biochemical and Molecular Medicine|April 1, 1996
Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for Genetic ServicesB L Therrell, W H Hannon, K A Pass, et al.Genomics|December 9, 2000
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiencyL Bartoloni, M Wattenhofer, J Kudoh, et al.Human Mutation|December 19, 2001
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenitaY H Zhang, B L Huang, K Anyane-Yeboa, et al.American Journal of Human Genetics|June 13, 1998
DAX1 mutations map to putative structural domains in a deduced three-dimensional modelY H Zhang, W Guo, R L Wagner, et al.Pageof 12