Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer

S Zhang, R Royer, S Li, JR McLaughlin, B Rosen… - Gynecologic …, 2011 - Elsevier
BACKGROUND: The heritable fraction of ovarian cancer exceeds that of any other common
adult cancer. Most inherited cases of ovarian cancer are due to a germline mutation in …
被引用次数：509 相关文章

Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer

S Zhang, R Royer, S Li, JR McLaughlin, B Rosen… - Gynecologic …, 2011 - infona.pl
The heritable fraction of ovarian cancer exceeds that of any other common adult cancer.
Most inherited cases of ovarian cancer are due to a germline mutation in BRCA1 or BRCA2 …

Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer

S Zhang, R Royer, S Li, JR McLaughlin… - Gynecologic …, 2011 - pubmed.ncbi.nlm.nih.gov
Background The heritable fraction of ovarian cancer exceeds that of any other common adult
cancer. Most inherited cases of ovarian cancer are due to a germline mutation in BRCA1 or …

Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer

S Zhang, R Royer, S Li… - Gynecologic …, 2011 - gynecologiconcology-online.net
Background The heritable fraction of ovarian cancer exceeds that of any other common adult
cancer. Most inherited cases of ovarian cancer are due to a germline mutation in BRCA1 or …

Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer.

S Zhang, R Royer, S Li, JR McLaughlin… - Gynecologic …, 2011 - europepmc.org
Background The heritable fraction of ovarian cancer exceeds that of any other common adult
cancer. Most inherited cases of ovarian cancer are due to a germline mutation in BRCA1 or …

[引用][C] Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer

S Zhang, R Royer, S Li, JR McLaughlin, B Rosen… - Gynecologic …, 2011 - cir.nii.ac.jp
Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive
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