Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1037, doi. 10.1007/s10038-006-0058-5
- By:
- Publication type:
- Article
Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 12
Results: 14
1
2
Replication of the association of the aspartic acid repeat polymorphism in the asporin gene with knee-osteoarthritis susceptibility in Han Chinese.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1068, doi. 10.1007/s10038-006-0065-6
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- Publication type:
- Article
3
A Japanese case of SCA14 with the Gly128Asp mutation.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1118, doi. 10.1007/s10038-006-0063-8
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- Publication type:
- Article
4
Association study of COL9A2 with lumbar disc disease in the Japanese population.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1063, doi. 10.1007/s10038-006-0062-9
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- Publication type:
- Article
5
Optimum two-stage designs in case–control association studies using false discovery rate.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1046, doi. 10.1007/s10038-006-0057-6
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- Publication type:
- Article
6
Gene–gene interaction between IL-13 and IL-13Rα1 is associated with total IgE in Korean children with atopic asthma.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1055, doi. 10.1007/s10038-006-0061-x
- By:
- Publication type:
- Article
7
Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1126, doi. 10.1007/s10038-006-0064-7
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- Publication type:
- Article
8
What is a ‘novel’ mtDNA mutation – and does ‘novelty’ really matter?
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1073, doi. 10.1007/s10038-006-0066-5
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- Publication type:
- Article
9
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.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1100, doi. 10.1007/s10038-006-0072-7
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- Publication type:
- Article
10
A silent polymorphism in the PER1 gene associates with extreme diurnal preference in humans.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1122, doi. 10.1007/s10038-006-0060-y
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- Publication type:
- Article
11
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1133, doi. 10.1007/s10038-006-0071-8
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- Publication type:
- Article
12
Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1087, doi. 10.1007/s10038-006-0070-9
- By:
- Publication type:
- Article
13
Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1110, doi. 10.1007/s10038-006-0073-6
- By:
- Publication type:
- Article
14
De novo 617G–A nucleotide mutation in the ACVR1 gene in a Taiwanese patient with fibrodysplasia ossificans progressiva.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1083, doi. 10.1007/s10038-006-0069-2
- By:
- Publication type:
- Article