Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 7
Results: 12
Obesity-related genetic variants, human pigmentation, and risk of melanoma.
- Published in:
- Human Genetics, 2013, v. 132, n. 7, p. 793, doi. 10.1007/s00439-013-1293-4
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- Publication type:
- Article
Sex- and age-dependent DNA methylation at the 17q12-q21 locus associated with childhood asthma.
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- Human Genetics, 2013, v. 132, n. 7, p. 811, doi. 10.1007/s00439-013-1298-z
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- Article
Replication of genetic loci for sarcoidosis in US black women: data from the Black Women's Health Study.
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- Human Genetics, 2013, v. 132, n. 7, p. 803, doi. 10.1007/s00439-013-1292-5
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- Publication type:
- Article
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study.
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- Human Genetics, 2013, v. 132, n. 7, p. 771, doi. 10.1007/s00439-013-1283-6
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- Article
Erratum to: Sex- and age-dependent DNA methylation at the 17q12-q21 locus associated with childhood asthma.
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- 2013
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- Publication type:
- Correction Notice
Victor McKusick and the history of medical genetics.
- Published in:
- 2013
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- Publication type:
- Book Review
Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.
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- Human Genetics, 2013, v. 132, n. 7, p. 783, doi. 10.1007/s00439-013-1294-3
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- Publication type:
- Article
Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective.
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- Human Genetics, 2013, v. 132, n. 7, p. 721, doi. 10.1007/s00439-013-1287-2
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- Publication type:
- Article
Recursive organizer (ROR): an analytic framework for sequence-based association analysis.
- Published in:
- Human Genetics, 2013, v. 132, n. 7, p. 745, doi. 10.1007/s00439-013-1285-4
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- Publication type:
- Article
Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes.
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- Human Genetics, 2013, v. 132, n. 7, p. 761, doi. 10.1007/s00439-013-1289-0
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- Publication type:
- Article
Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis.
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- Human Genetics, 2013, v. 132, n. 7, p. 825, doi. 10.1007/s00439-013-1296-1
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- Publication type:
- Article
Association between common alcohol dehydrogenase gene ( ADH) variants and schizophrenia and autism.
- Published in:
- Human Genetics, 2013, v. 132, n. 7, p. 735, doi. 10.1007/s00439-013-1277-4
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- Publication type:
- Article