MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation - Normandie Université Access content directly
Journal Articles Familial Cancer Year : 2016
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hal-02356387 , version 1 (08-11-2019)

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Aurélia Nguyen, Gaëlle Bougeard, Mériam Koob, Marie Pierre Chenard, Anne Schneider, et al.. MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation. Familial Cancer, 2016, 15 (4), pp.571-577. ⟨10.1007/s10689-016-9894-4⟩. ⟨hal-02356387⟩
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