Works matching IS 03406717 AND DT 2012 AND VI 131 AND IP 9
Results: 10
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction.
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- Human Genetics, 2012, v. 131, n. 9, p. 1519, doi. 10.1007/s00439-012-1180-4
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- Article
Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.
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- Human Genetics, 2012, v. 131, n. 9, p. 1403, doi. 10.1007/s00439-012-1174-2
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- Article
Recommendations for ethical approaches to genotype-driven research recruitment.
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- Human Genetics, 2012, v. 131, n. 9, p. 1423, doi. 10.1007/s00439-012-1177-z
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- Article
U-statistics in genetic association studies.
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- Human Genetics, 2012, v. 131, n. 9, p. 1395, doi. 10.1007/s00439-012-1178-y
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- Article
Genome-wide genetic associations with IFNγ response to smallpox vaccine.
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- Human Genetics, 2012, v. 131, n. 9, p. 1433, doi. 10.1007/s00439-012-1179-x
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- Article
Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts.
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- Human Genetics, 2012, v. 131, n. 9, p. 1453, doi. 10.1007/s00439-012-1182-2
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- Article
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium.
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- Human Genetics, 2012, v. 131, n. 9, p. 1467, doi. 10.1007/s00439-012-1176-0
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- Article
Identification of germline genomic copy number variation in familial pancreatic cancer.
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- Human Genetics, 2012, v. 131, n. 9, p. 1481, doi. 10.1007/s00439-012-1183-1
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- Article
Genome-wide association analysis of circulating vitamin D levels in children with asthma.
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- Human Genetics, 2012, v. 131, n. 9, p. 1495, doi. 10.1007/s00439-012-1185-z
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- Article
Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma.
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- Human Genetics, 2012, v. 131, n. 9, p. 1507, doi. 10.1007/s00439-012-1187-x
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- Article