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Germline TP5 3 mutations is common in patients with two early‐onset primary malignancies
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Published in: | Clinical genetics 2015-05, Vol.87 (5), p.499-501 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
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cited_by | cdi_FETCH-LOGICAL-c740-6f44ac5ffd7462ba9924d648007fbff068283a3b024f89dadfd73820fed2c8233 |
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cites | cdi_FETCH-LOGICAL-c740-6f44ac5ffd7462ba9924d648007fbff068283a3b024f89dadfd73820fed2c8233 |
container_end_page | 501 |
container_issue | 5 |
container_start_page | 499 |
container_title | Clinical genetics |
container_volume | 87 |
creator | Chak, B. P. Chan, E. S. Tong, J. H. Leung, A. W. Cheng, F. W. Lam, G. K. Shing, M. M. Li, C. K. To, K. F. |
description | |
doi_str_mv | 10.1111/cge.12480 |
format | article |
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language | eng |
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source | Wiley-Blackwell Read & Publish Collection |
title | Germline TP5 3 mutations is common in patients with two early‐onset primary malignancies |
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