Works matching IS 14345161 AND DT 2012 AND VI 57 AND IP 10
Results: 14
Genetic variants at 5p12 and risk of breast cancer in Han Chinese.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 638, doi. 10.1038/jhg.2012.83
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- Article
NDesign: software for study design for the detection of rare variants from next-generation sequencing data.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 676, doi. 10.1038/jhg.2012.81
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- Article
Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 665, doi. 10.1038/jhg.2012.94
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- Article
Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 654, doi. 10.1038/jhg.2012.90
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- Article
Paternal uniparental isodisomy of chromosome 22 in a patient with metachromatic leukodystrophy.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 687, doi. 10.1038/jhg.2012.97
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- Article
USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 633, doi. 10.1038/jhg.2012.79
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- Article
Genome-wide association study identifies GYS2 as a novel genetic factor for polycystic ovary syndrome through obesity-related condition.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 660, doi. 10.1038/jhg.2012.92
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- Article
DBGSA: a novel method of distance-based gene set analysis.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 642, doi. 10.1038/jhg.2012.86
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- Article
On the Y-chromosome haplogroup C3c classification.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 685, doi. 10.1038/jhg.2012.93
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- Article
A commentary on 'TECTA mutations in Japanese with mid-frequency hearing loss affected by Zona Pellucida domain protein secretion'.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 619, doi. 10.1038/jhg.2012.89
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- Article
Identification of ALK germline mutation (3605delG) in pediatric anaplastic medulloblastoma.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 682, doi. 10.1038/jhg.2012.87
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- Article
Hypermethylation of OPRM1 promoter region in European Americans with alcohol dependence.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 670, doi. 10.1038/jhg.2012.98
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- Article
Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 679, doi. 10.1038/jhg.2012.84
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- Publication type:
- Article
Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 10, p. 621, doi. 10.1038/jhg.2012.91
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- Article