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A frameshift mutation in exon 19 of MLH1 in a Chinese Lynch syndrome family: a pedigree study
lynch syndrome (LS), an autosomal dominantly inherited disease previously known as hereditary non-polyposis colorectal cancer (HNPCC), leads to a high risk of colorectal cancer (CRC) as well as malignancy at certain sites including endometrium, ovary, stomach, and small bowel (Hampel et al., 2008; L...
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| Publicado no: | J Zhejiang Univ Sci B |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Zhejiang University Press
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6331328/ https://ncbi.nlm.nih.gov/pubmed/30614234 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.B1800105 |
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