Frequency of the TP53 p.R337H mutation in a Brazilian cohort of pediatric patients with solid tumors-Reference-Cited by-同舟云学术

Frequency of the TP53 p.R337H mutation in a Brazilian cohort of pediatric patients with solid tumors

Published:2020-07-15 Issue:8 Volume:47 Page:6439-6443
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Feitosa José Antonio da Silva,das Chagas Pablo Ferreira,de Sousa Graziella Ribeiro,Queiroz Rosane Gomes de Paula,Cruzeiro Gustavo Alencastro Veiga,Tone Luiz Gonzaga,Borges Kleiton Silva^ORCID,Valera Elvis Terci

Funder

Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s11033-020-05655-5.pdf

Reference27 articles.

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3. Kratz CP, Achatz MI, Brugieres L et al (2017) Cancer screening recommendations for individuals with Li–Fraumeni syndrome. Clin Cancer Res. https://doi.org/10.1158/1078-0432.CCR-17-0408

4. Bougeard G, Renaux-Petel M, Flaman JM et al (2015) Revisiting Li–Fraumeni syndrome from TP53 mutation carriers. J Clin Oncol. https://doi.org/10.1200/JCO.2014.59.5728

5. Borges LM, Ayres FM (2015) R337H mutation of the TP53 gene as a clinical marker in cancer patients: a systematic review of literature. Genet Mol Res. https://doi.org/10.4238/2015.December.16.4

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