Composite Adrenocortical Carcinoma and Neuroblastoma in an Infant With a TP53 Germline Mutation: A Case Report and Literature Review-Reference-Cited by-同舟云学术

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Composite Adrenocortical Carcinoma and Neuroblastoma in an Infant With a TP53 Germline Mutation: A Case Report and Literature Review

Published:2019-07 Issue:5 Volume:41 Page:399-401
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Tang Yue-Jia,Yu Ting-Ting,Ma Jing,Zhou Ying,Xu Min,Gao Yi-Jin

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference21 articles.

1. Germline TP53 mutations and the changing landscape of Li-Fraumeni syndrome;Kamihara;Hum Mutat,2014

2. Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children’s oncology group study;Wasserman;J Clin Oncol,2015

3. 2009 version of the Chompret criteria for Li Fraumeni syndrome;Tinat;J Clin Oncol,2009

4. Sensitivity and predictive value of criteria for p53 germline mutation screening;Chompret;J Med Genet,2001

5. Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families;Bougeard;J Med Genet,2008

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Molecular genotyping of adrenocortical carcinoma: a systematic analysis of published literature 2019–2021;Current Opinion in Oncology;2021-10-19

2. Adrenocortical Carcinoma: Updates of Clinical and Pathological Features after Renewed World Health Organisation Classification and Pathology Staging;Biomedicines;2021-02-10

3. A case of synchronous malignancy with novel missense mutation in a child: Is this Li-Fraumeni syndrome or a novel case masquerading as Li-Fraumeni syndrome??;Indian Journal of Medical and Paediatric Oncology;2020-09

4. The function of a heterozygous p53 mutation in a Li-Fraumeni syndrome patient;PLOS ONE;2020-06-09

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