CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
about
Identification of a novel CHEK2 variant and assessment of its contribution to the risk of breast cancer in French Canadian women.Current perspectives on CHEK2 mutations in breast cancer.The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population.CHEK2 contribution to hereditary breast cancer in non-BRCA familiesRAD51 135G>C and TP53 Arg72Pro polymorphisms and susceptibility to breast cancer in Serbian women
P2860
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
@ast
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
@en
type
label
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
@ast
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
@en
prefLabel
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
@ast
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
@en
P2860
P356
P1433
P1476
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.
@en
P2093
Hans Eiberg
Marie Luise Bisgaard
P2860
P2888
P356
10.1186/1471-2407-7-163
P407
P577
2007-08-17T00:00:00Z
P5875
P6179
1027097668