Works matching IS 14345161 AND DT 2004 AND VI 49 AND IP 12
Results: 8
Association analysis ofSLC22A4,SLC22A5andDLG5in Japanese patients with Crohn disease.
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- Journal of Human Genetics, 2004, v. 49, n. 12, p. 664, doi. 10.1007/s10038-004-0204-x
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- Article
The role ofHFEmutations on iron metabolism in beta-thalassemia carriers.
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- Journal of Human Genetics, 2004, v. 49, n. 12, p. 651, doi. 10.1007/s10038-004-0202-z
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- Article
Molecular screening of the microsomal triglyceride transfer protein: association between polymorphisms and both abdominal obesity and plasma apolipoprotein B concentration.
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- Journal of Human Genetics, 2004, v. 49, n. 12, p. 684, doi. 10.1007/s10038-004-0207-7
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- Article
Association of an intragenic microsatellite marker in theCC16gene with asthma in the Indian population.
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- Journal of Human Genetics, 2004, v. 49, n. 12, p. 677, doi. 10.1007/s10038-004-0206-8
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- Article
Population prevalence of APOE, APOC3 and PPAR-a mutations associated to hypertriglyceridemia in French Canadians.
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- Journal of Human Genetics, 2004, v. 49, n. 12, p. 691, doi. 10.1007/s10038-004-0208-6
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- Article
Clinical, biochemical, and cytochemical studies on a Japanese Salla disease case associated with a renal disorder.
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- Journal of Human Genetics, 2004, v. 49, n. 12, p. 656, doi. 10.1007/s10038-004-0203-y
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- Article
mtDNA/nDNA ratio in 14484 LHON mitochondrial mutation carriers.
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- Journal of Human Genetics, 2004, v. 49, n. 12, p. 701, doi. 10.1007/s10038-004-0209-5
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- Article
Designing a multistage,SNP-based,genome screen for common diseases.
- Published in:
- Journal of Human Genetics, 2004, v. 49, n. 12, p. 669, doi. 10.1007/s10038-004-0205-9
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- Article