Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 2
Results: 12
Novel mutations in the cytochrome P450 2C19 gene: a pitfall of the PCR-RFLP method for identifying a common mutation.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 118, doi. 10.1007/s10038-005-0332-y
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High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 151, doi. 10.1007/s10038-005-0337-6
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- Article
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 98, doi. 10.1007/s10038-005-0329-6
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- Article
Polymorphisms in the leptin receptor (LEPR)—putative association with obesity and T2DM.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 85, doi. 10.1007/s10038-005-0327-8
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Exogenous gene expression and growth regulation of hematopoietic cells via a novel human artificial chromosome.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 147, doi. 10.1007/s10038-005-0334-9
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The hOGG1 Ser<sup>326</sup>Cys gene polymorphism is associated with decreased insulin sensitivity in subjects with normal glucose tolerance.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 124, doi. 10.1007/s10038-005-0335-8
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Androgen receptor CAG and GGC polymorphisms in Mediterraneans: repeat dynamics and population relationships.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 129, doi. 10.1007/s10038-005-0336-7
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Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 141, doi. 10.1007/s10038-005-0333-x
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- Article
ALDH2 and CYP2E1 genotypes, urinary acetaldehyde excretion and the health consequences in moderate alcohol consumers.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 104, doi. 10.1007/s10038-005-0330-0
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- Article
Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuoles.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 137, doi. 10.1007/s10038-005-0338-5
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- Article
Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 112, doi. 10.1007/s10038-005-0331-z
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- Article
A novel Wiskott-Aldrich syndrome protein (WASP) complex mutation identified in a WAS patient results in an aberrant product at the C-terminus from two transcripts with unusual polyA signals.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 92, doi. 10.1007/s10038-005-0328-7
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- Article