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MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation

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https://hal-normandie-univ.archives-ouvertes.fr/hal-02356387
Contributor : Gaëlle Bougeard <>
Submitted on : Friday, November 8, 2019 - 4:57:34 PM
Last modification on : Monday, June 29, 2020 - 12:08:06 PM

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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, Springer Verlag (Germany), 2016, 15 (4), pp.571-577. ⟨10.1007/s10689-016-9894-4⟩. ⟨hal-02356387⟩

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