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Lynch Syndrome Screening Should Be Considered for All Patients With Newly Diagnosed Endometrial Cancer

Lynch syndrome (LS) is an autosomal dominant inherited disorder caused by germline mutations in DNA mismatch repair (MMR) genes. Mutation carriers are at substantially increased risk of developing cancers of the colorectum and endometrium, among others. Given recent recommendations for universal, co...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Am J Surg Pathol
Päätekijät: Mills, Anne M., Liou, Sofia, Ford, James M., Berek, Jonathan S., Pai, Reetesh K., Longacre, Teri A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2014
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4361228/
https://ncbi.nlm.nih.gov/pubmed/25229768
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAS.0000000000000321
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