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
2016 ◽
Vol 14
(1)
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2018 ◽
Vol 101
(5)
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pp. 938-944
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2020 ◽
Vol 83
(6)
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pp. AB34
2010 ◽
Vol 37
(1)
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pp. 109-133
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2020 ◽
Vol 180
(2)
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pp. 511-514
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2015 ◽
Vol 33
(15_suppl)
◽
pp. e12509-e12509
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