Works matching IS 03406717 AND DT 2006 AND VI 119 AND IP 4
Results: 13
Archives and human genetics: saving the past for the future.
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- Human Genetics, 2006, v. 119, n. 4, p. 459, doi. 10.1007/s00439-005-0110-0
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Interferon gamma polymorphisms and their interaction with smoking are associated with lung function.
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- Human Genetics, 2006, v. 119, n. 4, p. 365, doi. 10.1007/s00439-006-0143-z
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Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses.
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- Human Genetics, 2006, v. 119, n. 4, p. 376, doi. 10.1007/s00439-006-0135-z
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Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man.
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- Human Genetics, 2006, v. 119, n. 4, p. 444, doi. 10.1007/s00439-006-0157-6
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Seventh international meeting on single nucleotide polymorphism and complex genome analysis: ‘ever bigger scans and an increasingly variable genome’.
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- Human Genetics, 2006, v. 119, n. 4, p. 451, doi. 10.1007/s00439-006-0151-z
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Long-term persistence of both functional and non-functional alleles at the leukocyte immunoglobulin-like receptor A3 ( LILRA3) locus suggests balancing selection.
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- Human Genetics, 2006, v. 119, n. 4, p. 436, doi. 10.1007/s00439-006-0152-y
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Evolutionary evidence suggests that CpG island-associated Alus are frequently unmethylated in human germline.
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- Human Genetics, 2006, v. 119, n. 4, p. 457, doi. 10.1007/s00439-006-0161-x
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Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12.
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- Human Genetics, 2006, v. 119, n. 4, p. 400, doi. 10.1007/s00439-006-0149-6
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Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number.
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- Human Genetics, 2006, v. 119, n. 4, p. 422, doi. 10.1007/s00439-006-0156-7
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Missense mutations in the BMP15 gene are associated with ovarian failure.
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- Human Genetics, 2006, v. 119, n. 4, p. 408, doi. 10.1007/s00439-006-0150-0
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A functional polymorphism in the PTHR1 promoter region is associated with adult height and BMD measured at the femoral neck in a large cohort of young caucasian women.
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- Human Genetics, 2006, v. 119, n. 4, p. 416, doi. 10.1007/s00439-006-0155-8
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Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36.
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- Human Genetics, 2006, v. 119, n. 4, p. 389, doi. 10.1007/s00439-006-0153-x
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Ascertainment adjustment in genetic studies of ordinal traits.
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- Human Genetics, 2006, v. 119, n. 4, p. 429, doi. 10.1007/s00439-006-0147-8
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- Article