Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 12
Results: 14
Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1037, doi. 10.1007/s10038-006-0058-5
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- Article
Replication of the association of the aspartic acid repeat polymorphism in the asporin gene with knee-osteoarthritis susceptibility in Han Chinese.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1068, doi. 10.1007/s10038-006-0065-6
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- Article
A Japanese case of SCA14 with the Gly128Asp mutation.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1118, doi. 10.1007/s10038-006-0063-8
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- Article
Association study of COL9A2 with lumbar disc disease in the Japanese population.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1063, doi. 10.1007/s10038-006-0062-9
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- Article
Optimum two-stage designs in case–control association studies using false discovery rate.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1046, doi. 10.1007/s10038-006-0057-6
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- Article
Gene–gene interaction between IL-13 and IL-13Rα1 is associated with total IgE in Korean children with atopic asthma.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1055, doi. 10.1007/s10038-006-0061-x
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- Article
Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1126, doi. 10.1007/s10038-006-0064-7
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- Article
What is a ‘novel’ mtDNA mutation – and does ‘novelty’ really matter?
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1073, doi. 10.1007/s10038-006-0066-5
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- Article
Effect of +36T > C in intron 1 on the glutamine: fructose-6-phosphate amidotransferase 1 gene and its contribution to type 2 diabetes in different populations.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1100, doi. 10.1007/s10038-006-0072-7
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- Article
A silent polymorphism in the PER1 gene associates with extreme diurnal preference in humans.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1122, doi. 10.1007/s10038-006-0060-y
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- Article
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1133, doi. 10.1007/s10038-006-0071-8
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- Article
Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1087, doi. 10.1007/s10038-006-0070-9
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- Article
Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1110, doi. 10.1007/s10038-006-0073-6
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- Article
De novo 617G–A nucleotide mutation in the ACVR1 gene in a Taiwanese patient with fibrodysplasia ossificans progressiva.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1083, doi. 10.1007/s10038-006-0069-2
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- Article