CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women-Reference-Cited by-同舟云学术

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CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women

Published:2011-11-05 Issue:12 Volume:48 Page:860-863
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Adank M. A.,Jonker M. A.,Kluijt I.,van Mil S. E.,Oldenburg R. A.,Mooi W. J.,Hogervorst F. B. L.,van den Ouweland A. M. W.,Gille J. J. P.,Schmidt M. K.,van der Vaart A. W.,Meijers-Heijboer H.,Waisfisz Q.

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 66 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. Clinical Impact of Constitutional Genomic Testing on Current Breast Cancer Care;Clinical Oncology;2024-08

2. The heterogeneous cancer phenotype of individuals with biallelic germline pathogenic variants in CHEK2;Genetics in Medicine;2024-05

3. Genetic Basis of Breast and Ovarian Cancer: Approaches and Lessons Learnt from Three Decades of Inherited Predisposition Testing;Genes;2024-02-08

4. Clinicopathologic and genetic analysis of invasive breast carcinomas in women with germline CHEK2 variants;Breast Cancer Research and Treatment;2023-12-13

5. Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG);Genetics in Medicine;2023-10

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