The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations-Reference-Cited by-同舟云学术

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The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations

Published:2014 Issue:1 Volume:9 Page:63
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

Silva Amanda G,Krepischi Ana CV,Pearson Peter L,Hainaut Pierre,Rosenberg Carla,Achatz Maria

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference24 articles.

1. Relative frequency and morphology of cancers in carriers of germline TP53 mutations

2. Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms

3. Highly penetrant hereditary cancer syndromes

4. Germline copy number variation and cancer risk

5. Germline copy number variations and cancer predisposition

Cited by 11 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. Unusual course of disease and genetic profile in Li-Fraumeni syndrome-associated osteosarcoma – a case report;Hereditary Cancer in Clinical Practice;2021-10-20

2. Identification of a Novel Mutation in Hereditary Breast Cancer in a Family with Wide Spectrum of Atypical Malignancies;Eurasian Journal of Medicine and Oncology;2021

3. Cancer and genomic instability;Genome Stability;2021

4. Frequency of the TP53 R337H variant in sporadic breast cancer and its impact on genomic instability;Scientific Reports;2020-10-06

5. Pediatric cancer genetics;Current Opinion in Pediatrics;2017-12

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