Works matching IS 14345161 AND DT 2003 AND VI 48 AND IP 8
Results: 9
Genomic structure and alternative splicing of the insulin receptor tyrosine kinase substrate of 53-kDa protein.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 410, doi. 10.1007/s10038-003-0047-x
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A Biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A→C is a mutation.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 399, doi. 10.1007/s10038-003-0044-0
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Identification of a novel 2026G→C mutation of the MRP2 gene in a Japanese patient with Dubin-Johnson syndrome.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 425, doi. 10.1007/s10038-003-0052-0
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Linkage and association of the CA repeat polymorphism of the IL6 gene, obesity-related phenotypes, and bone mineral density (BMD) in two independent Caucasian populations.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 430, doi. 10.1007/s10038-003-0053-z
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DNA polymorphisms of lipase related genes.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 443, doi. 10.1007/s10038-003-0051-1
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Genetic deficiency of a mitochondrial aldehyde dehydrogenase increases serum lipid peroxides in community-dwelling females.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 404, doi. 10.1007/s10038-003-0046-y
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A novel locus for parietal foramina maps to chromosome 4q21-q23.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 420, doi. 10.1007/s10038-003-0050-2
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Identification of a novel candidate gene in the iron-sulfur pathway implicated in ataxia-susceptibility: human gene encoding HscB, a J-type co-chaperone.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 415, doi. 10.1007/s10038-003-0048-9
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Cloning and identification of the human LPAAT-zeta gene, a novel member of the lysophosphatidic acid acyltransferase family.
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- Journal of Human Genetics, 2003, v. 48, n. 8, p. 438, doi. 10.1007/s10038-003-0045-z
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- Article