Expanding the genetic basis of copy number variation in familial breast cancer.
about
NCG 5.0: updates of a manually curated repository of cancer genes and associated properties from cancer mutational screenings.WWOX CNV-67048 Functions as a Risk Factor for Epithelial Ovarian Cancer in Chinese Women by Negatively Interacting with Oral Contraceptive Use.Germline large genomic alterations on 7q in patients with multiple primary cancers.BCIP: a gene-centered platform for identifying potential regulatory genes in breast cancer.Characterization of potential driver mutations involved in human breast cancer by computational approaches.Germline copy number variations are associated with breast cancer risk and prognosis.
P2860
Expanding the genetic basis of copy number variation in familial breast cancer.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Expanding the genetic basis of copy number variation in familial breast cancer.
@ast
Expanding the genetic basis of copy number variation in familial breast cancer.
@en
type
label
Expanding the genetic basis of copy number variation in familial breast cancer.
@ast
Expanding the genetic basis of copy number variation in familial breast cancer.
@en
prefLabel
Expanding the genetic basis of copy number variation in familial breast cancer.
@ast
Expanding the genetic basis of copy number variation in familial breast cancer.
@en
P2093
P2860
P356
P1476
Expanding the genetic basis of copy number variation in familial breast cancer
@en
P2093
Amy L Masson
Desma M Grice
Garry N Hannan
Rodney J Scott
Tiffany-Jane Evans
P2860
P2888
P356
10.1186/1897-4287-12-15
P577
2014-05-24T00:00:00Z
P5875
P6179
1017232596