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Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 11, p. 755, doi. 10.1038/jhg.2011.95
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- Article
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 759, doi. 10.1038/jhg.2011.96
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- Article
Y-chromosome haplogroup diversity in the sub-Himalayan Terai and Duars populations of East India.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 765, doi. 10.1038/jhg.2011.98
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- Article
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 772, doi. 10.1038/jhg.2011.99
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- Article
Gene expression analysis in lymphoblastoid cells as a potential biomarker of bipolar disorder.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 779, doi. 10.1038/jhg.2011.101
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- Article
HVS-I polymorphism screening of ancient human mitochondrial DNA provides evidence for N9a discontinuity and East Asian haplogroups in the Neolithic Hungary.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 11, p. 784, doi. 10.1038/jhg.2011.103
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- Article
UBE3C genetic variations as potent markers of nasal polyps in Korean asthma patients.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 797, doi. 10.1038/jhg.2011.104
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- Article
Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 801, doi. 10.1038/jhg.2011.105
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- Article
Support for association between the Ser205Leu polymorphism of p75<sup>NTR</sup> and major depressive disorder.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 806, doi. 10.1038/jhg.2011.107
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- Article
Tandem configurations of variably duplicated segments of 22q11.2 confirmed by fiber-FISH analysis.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 11, p. 810, doi. 10.1038/jhg.2011.100
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- Article