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BRCA1 and BRCA2 Mutations Other Than the Founder Alleles Among Ashkenazi Jewish in the Population of Argentina

In Ashkenazi Jewish (AJ) high risk families 3 mutations [2 in BRCA1 (c. 68_69del and c.5266dup) and 1 in BRCA2 (c.5946del)] account for the majority of high risk breast and ovarian cancer cases in that ethnic group. Few studies with limited number of genotyped individuals have expanded the spectrum...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Oncol
Prif Awduron: Solano, Angela R., Liria, Natalia C., Jalil, Fernanda S., Faggionato, Daniela M., Mele, Pablo G., Mampel, Alejandra, Cardoso, Florencia C., Podesta, Ernesto J.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2018
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6113569/
https://ncbi.nlm.nih.gov/pubmed/30186769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fonc.2018.00323
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