Works matching IS 14345161 AND DT 2008 AND VI 53 AND IP 10
Results: 14
Genetic interactions model among Eotaxin gene polymorphisms in asthma.
- Published in:
- Journal of Human Genetics, 2008, v. 53, n. 10, p. 867, doi. 10.1007/s10038-008-0314-y
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- Article
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan ( SGCE) gene.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 876, doi. 10.1007/s10038-008-0321-z
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Appropriate data cleaning methods for genome-wide association study.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 886, doi. 10.1007/s10038-008-0322-y
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- Article
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 894, doi. 10.1007/s10038-008-0323-x
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Pharmacokinetic interaction between pravastatin and olmesartan in relation to SLCO1B1 polymorphism.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 899, doi. 10.1007/s10038-008-0324-9
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Genetic imprint of the Mongol: signal from phylogeographic analysis of mitochondrial DNA.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 905, doi. 10.1007/s10038-008-0325-8
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- Article
Case report of de novo dup(18p)/del(18q) and r(18) mosaicism.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 941, doi. 10.1007/s10038-008-0326-7
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- Article
Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 914, doi. 10.1007/s10038-008-0327-6
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- Article
The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease).
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 947, doi. 10.1007/s10038-008-0328-5
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- Article
Monozygotic female twins discordant for Silver–Russell syndrome and hypomethylation of the H19-DMR.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 950, doi. 10.1007/s10038-008-0329-4
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Analysis of segregation patterns in Machado–Joseph disease pedigrees.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 920, doi. 10.1007/s10038-008-0330-y
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- Article
Mitochondrial DNA variant interactions modify breast cancer risk.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 924, doi. 10.1007/s10038-008-0331-x
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- Article
Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 929, doi. 10.1007/s10038-008-0332-9
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- Article
NEFL Pro22Arg mutation in Charcot-Marie-Tooth disease type 1.
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- Journal of Human Genetics, 2008, v. 53, n. 10, p. 936, doi. 10.1007/s10038-008-0333-8
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- Article