Works matching IS 14345161 AND DT 2010 AND VI 55 AND IP 2
Results: 12
CFTR allelic heterogeneity in Brazil: historical and geographical perspectives and implications for screening and counseling for cystic fibrosis in this country.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 71, doi. 10.1038/jhg.2009.123
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Differential expression of a subset of ribosomal protein genes in cell lines derived from human nasopharyngeal epithelium.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 118, doi. 10.1038/jhg.2009.124
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Correlation of genotypes for thiopurine methyltransferase and inosine triphosphate pyrophosphatase with long-term clinical outcomes in Korean patients with inflammatory bowel diseases during treatment with thiopurine drugs.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 121, doi. 10.1038/jhg.2009.125
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Replication of a genome-wide association study of panic disorder in a Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 91, doi. 10.1038/jhg.2009.127
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Alcohol dehydrogenase-2 and aldehyde dehydrogenase-2 genotypes, alcohol drinking and the risk for esophageal cancer in a Chinese population.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 97, doi. 10.1038/jhg.2009.129
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Inheritance of a novel mutated allele of the OCA2 gene associated with high incidence of oculocutaneous albinism in a Polynesian community.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 103, doi. 10.1038/jhg.2009.130
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A type of familial cleft of the soft palate maps to 2p24.2–p24.1 or 2p21–p12.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 124, doi. 10.1038/jhg.2009.131
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Novel deletions causing pseudoxanthoma elasticum underscore the genomic instability of the ABCC6 region.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 112, doi. 10.1038/jhg.2009.132
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Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 127, doi. 10.1038/jhg.2009.133
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A genome-wide scan of male sexual orientation.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 131, doi. 10.1038/jhg.2009.135
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Recent advances in association studies of osteoarthritis susceptibility genes.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 77, doi. 10.1038/jhg.2009.137
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Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 81, doi. 10.1038/jhg.2009.138
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- Article