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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Front Oncol
मुख्य लेखकों: Solano, Angela R., Liria, Natalia C., Jalil, Fernanda S., Faggionato, Daniela M., Mele, Pablo G., Mampel, Alejandra, Cardoso, Florencia C., Podesta, Ernesto J.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Frontiers Media S.A. 2018
विषय:
ऑनलाइन पहुंच: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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