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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

作者：Rashid Muhammad U; Naeemi Humaira; Muhammad Noor; Loya Asif; Yusuf Muhammed A; Lubinski Jan; Jakubowska Anna; Hamann Ute
来源：Hereditary Cancer in Clinical Practice, 2016, 14(1): 14.
DOI：10.1186/s13053-016-0056-3
  • 出版日期2016-7-12

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更新时间：2021-03-27 16:56