Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 4
Results: 15
Identification of probable genotyping errors by consideration of haplotypes.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 450, doi. 10.1038/sj.ejhg.5201565
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Association study of major risk single nucleotide polymorphisms in the common regulatory region of PARK2 and PACRG genes with leprosy in an Indian population.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 438, doi. 10.1038/sj.ejhg.5201563
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Ovarian Cancer: Identification of remodeling and spacing factor 1 (rsf-1, HBXAP) at chromosome 11q13 as a putative oncogene in ovarian cancer.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 381, doi. 10.1038/sj.ejhg.5201570
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Influence of serotonin receptor 2A His452Tyr polymorphism on brain temporal structures: a volumetric MR study.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 443, doi. 10.1038/sj.ejhg.5201573
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Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesis.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 403, doi. 10.1038/sj.ejhg.5201574
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Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 459, doi. 10.1038/sj.ejhg.5201576
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Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 497, doi. 10.1038/sj.ejhg.5201578
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It's ‘back to school’ for genetic screening.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 384, doi. 10.1038/sj.ejhg.5201581
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The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 469, doi. 10.1038/sj.ejhg.5201582
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An utter refutation of the ‘Fundamental Theorem of the HapMap’.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 426, doi. 10.1038/sj.ejhg.5201583
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Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 390, doi. 10.1038/sj.ejhg.5201584
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3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 478, doi. 10.1038/sj.ejhg.5201589
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Role of interferon-γ gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 488, doi. 10.1038/sj.ejhg.5201591
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Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 410, doi. 10.1038/sj.ejhg.5201592
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Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 418, doi. 10.1038/sj.ejhg.5201593
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