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