Works matching IS 10184813 AND DT 2007 AND VI 15 AND IP 3
Results: 21
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 260, doi. 10.1038/sj.ejhg.5201753
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Sotos syndrome.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 264, doi. 10.1038/sj.ejhg.5201686
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Cystic Fibrosis: Cystic fibrosis and lactase persistence: a possible correlation.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 255, doi. 10.1038/sj.ejhg.5201749
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Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 302, doi. 10.1038/sj.ejhg.5201751
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Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 313, doi. 10.1038/sj.ejhg.5201752
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No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 320, doi. 10.1038/sj.ejhg.5201754
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Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 328, doi. 10.1038/sj.ejhg.5201756
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Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 347, doi. 10.1038/sj.ejhg.5201757
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Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 375, doi. 10.1038/sj.ejhg.5201758
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Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 352, doi. 10.1038/sj.ejhg.5201759
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Multiple mutations responsible for frequent genetic diseases in isolated populations.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 272, doi. 10.1038/sj.ejhg.5201760
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A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 362, doi. 10.1038/sj.ejhg.5201761
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FGF10 missense mutations in aplasia of lacrimal and salivary glands (ALSG).
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 379, doi. 10.1038/sj.ejhg.5201762
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Dopamine transporter, gender, and number of sexual partners among young adults.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 279, doi. 10.1038/sj.ejhg.5201763
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Partial duplications of the MSH2 and MLH1 genes in hereditary nonpolyposis colorectal cancer.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 383, doi. 10.1038/sj.ejhg.5201765
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Haplotypes in the human Foxo1a and Foxo3a genes; impact on disease and mortality at old age.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 294, doi. 10.1038/sj.ejhg.5201766
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Association of PDCD1 polymorphisms with childhood-onset systemic lupus erythematosus.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 336, doi. 10.1038/sj.ejhg.5201767
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Africans in Yorkshire? The deepest-rooting clade of the Y phylogeny within an English genealogy.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 288, doi. 10.1038/sj.ejhg.5201771
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Progranulin mutations in Dutch familial frontotemporal lobar degeneration.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 369, doi. 10.1038/sj.ejhg.5201772
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TCF7L2 polymorphisms are associated with type 2 diabetes in northern Sweden.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 342, doi. 10.1038/sj.ejhg.5201773
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AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.
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- 2007
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