Contiguous Gene Deletion of Chromosome 2p16.3-p21 as a Cause of Lynch Syndrome

Lynch syndrome is an autosomal dominant condition caused by pathogenic mutations in the DNA mismatch repair (MMR) genes. Although commonly associated with clinical features such as intellectual disability and congenital anomalies, contiguous gene deletions may also result in cancer predisposition sy...

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Publicado en:Fam Cancer
Autores principales: Salo-Mullen, Erin E., Lynn, Patricio B., Wang, Lu, Walsh, Michael, Gopalan, Anuradha, Shia, Jinru, Tran, Christina, Man, Fung Ying, McBride, Sean, Schattner, Mark, Zhang, Liying, Weiser, Martin R., Stadler, Zsofia K.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2018
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5708147/
https://ncbi.nlm.nih.gov/pubmed/28555354
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10689-017-0006-x
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