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Comment
. 2019 Nov;21(11):2652-2653.
doi: 10.1038/s41436-019-0530-1. Epub 2019 May 2.

Response to Yang et al

Affiliations
Free article
Comment

Response to Yang et al

A Olkinuora et al. Genet Med. 2019 Nov.
Free article
No abstract available

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References

    1. Olkinuora A, Nieminen TT, Mårtensson E, et al. Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition. Genet Med. 2018 Dec 21; https://doi.org/10.1038/s41436-018-0405-x [Epub ahead of print].
    1. Yang M, Zhu L, Xu D, et al. Response to Olkinuora et al. 2018: How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer? Genet Med. 2019; https://doi.org/10.1038/s41436-019-0529-7 [Epub ahead of print].
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    1. Goodenberger ML, Thomas BC, Riefert-Johnson D, et al. PMS2 monoallelic mutation carriers: the known unknown. Genet Med. 2016;18:13–19. - DOI
    1. Levi Z, Kariv R, Barnes-Kedar I, et al. The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer. Clin Genet. 2015;88:474–478. - DOI

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