Found: 14
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Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 809, doi. 10.1038/jhg.2012.132
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- Publication type:
- Article
Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 776, doi. 10.1038/jhg.2012.110
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- Publication type:
- Article
A commentary on the history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations.
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- Journal of Human Genetics, 2012, v. 57, n. 12, p. 753, doi. 10.1038/jhg.2012.121
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- Article
Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 772, doi. 10.1038/jhg.2012.109
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- Article
A Commentary on Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1.
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- Journal of Human Genetics, 2012, v. 57, n. 12, p. 755, doi. 10.1038/jhg.2012.122
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- Publication type:
- Article
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 810, doi. 10.1038/jhg.2012.125
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- Publication type:
- Article
A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 766, doi. 10.1038/jhg.2012.108
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- Publication type:
- Article
Pentanucleotide repeat-primed PCR for genetic diagnosis of spinocerebellar ataxia type 31.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 807, doi. 10.1038/jhg.2012.112
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- Publication type:
- Article
Tandem repeat sequences evolutionarily related to SVA-type retrotransposons are expanded in the centromere region of the western hoolock gibbon, a small ape.
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- Journal of Human Genetics, 2012, v. 57, n. 12, p. 760, doi. 10.1038/jhg.2012.107
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- Article
Is the prevalence of MTHFR C677T polymorphism associated with ultraviolet radiation in Eurasia?
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- Journal of Human Genetics, 2012, v. 57, n. 12, p. 780, doi. 10.1038/jhg.2012.113
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- Publication type:
- Article
Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 756, doi. 10.1038/jhg.2012.103
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- Publication type:
- Article
Sibling cases of moyamoya disease having homozygous and heterozygous c.14576G>A variant in RNF213 showed varying clinical course and severity.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 804, doi. 10.1038/jhg.2012.105
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- Publication type:
- Article
The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 787, doi. 10.1038/jhg.2012.114
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- Publication type:
- Article
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 12, p. 796, doi. 10.1038/jhg.2012.120
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- Publication type:
- Article