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Comment
. 2019 Nov;21(11):2650-2651.
doi: 10.1038/s41436-019-0529-7. Epub 2019 May 2.

How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer?

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Free article
Comment

How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer?

Mengyuan Yang et al. Genet Med. 2019 Nov.
Free article
No abstract available

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Comment in

  • Response to Yang et al.
    Olkinuora A, Nieminen TT, Nordling M, Peltomäki P. Olkinuora A, et al. Genet Med. 2019 Nov;21(11):2652-2653. doi: 10.1038/s41436-019-0530-1. Epub 2019 May 2. Genet Med. 2019. PMID: 31043712 No abstract available.

Comment on

  • Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition.
    Olkinuora A, Nieminen TT, Mårtensson E, Rohlin A, Ristimäki A, Koskenvuo L, Lepistö A; Swedish Extended Genetic Analysis of Colorectal Neoplasia (SWEN) Study Group; Gebre-Medhin S, Nordling M, Peltomäki P. Olkinuora A, et al. Genet Med. 2019 Aug;21(8):1868-1873. doi: 10.1038/s41436-018-0405-x. Epub 2018 Dec 21. Genet Med. 2019. PMID: 30573798 Free PMC article.

References

Reference

    1. Olkinuora A, 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].

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