A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome
暂无分享,去创建一个
U. Hamann | A. Jakubowska | J. Lubiński | M. A. Yusuf | N. Muhammad | H. Naeemi | M. U. Rashid | A. Loya