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Determining the frequency of de novo germline mutations in DNA mismatch repair genes

BACKGROUND: Carriers of a germline mutation in a DNA mismatch repair (MMR) gene—that is, persons with Lynch syndrome—have substantially high risks of colorectal (CRC), endometrial, and several other cancers. The proportion of carriers who have de novo mutations (not inherited from either parent) is...

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Main Authors: Win, Aung Ko, Jenkins, Mark A, Buchanan, Daniel D, Clendenning, Mark, Young, Joanne P, Giles, Graham G, Goldblatt, Jack, Leggett, Barbara A, Hopper, John L, Thibodeau, Stephen N, Lindor, Noralane M
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2011
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3436601/
https://ncbi.nlm.nih.gov/pubmed/21636617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2011-100082
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