TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge

PURPOSE: TP53germline (g) mutations, associated with the Li-Fraumeni syndrome (LFS), have rarely been reported in the context of hereditary breast and ovarian cancer (HBOC). The prevalence and cancer risks in this target group are unknown and counseling remains challenging. Notably an extensive high...

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Detalhes bibliográficos
Publicado no:Arch Gynecol Obstet
Main Authors: Grill, Sabine, Ramser, Juliane, Hellebrand, Heide, Pfarr, Nicole, Boxberg, Melanie, Brambs, Christine, Ditsch, Nina, Meindl, Alfons, Groß, Eva, Meitinger, Thomas, Kiechle, Marion, Quante, Anne S.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2020
Assuntos:
Gynecologic Oncology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8087555/
https://ncbi.nlm.nih.gov/pubmed/33245408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00404-020-05883-x
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