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Identification of functionally active, low frequency copy number variants at 15q21.3 and 12q21.31 associated with prostate cancer risk.
Proc Natl Acad Sci U S A ; 109(17): 6686-91, 2012 Apr 24.
Article in En | MEDLINE | ID: mdl-22496589

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Chromosomes, Human, Pair 12 / Chromosomes, Human, Pair 15 / Gene Dosage / Genetic Predisposition to Disease Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Proc Natl Acad Sci U S A Year: 2012 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Chromosomes, Human, Pair 12 / Chromosomes, Human, Pair 15 / Gene Dosage / Genetic Predisposition to Disease Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Proc Natl Acad Sci U S A Year: 2012 Type: Article Affiliation country: United States