Papillary thyroid cancer in a patient with germline CHEK2 mutation: A case report
- 21 September 2021
- journal article
- letter
- Published by Elsevier in Annales d'Endocrinologie
- Vol. 82 (6) , 624-626
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Coexisting Germline CHEK2 and Somatic BRAFV600E Mutations in Papillary Thyroid Cancer and Their Association with Clinicopathological Features and Disease CourseCancers, 2019
- Identification of Rare Variants Predisposing to Thyroid CancerThyroid®, 2019
- The c.470 T > C CHEK2 missense variant increases the risk of differentiated thyroid carcinoma in the Great Poland populationHereditary Cancer in Clinical Practice, 2015
- CHEK2mutations and the risk of papillary thyroid cancerInternational Journal of Cancer, 2015
- Integrated Genomic Characterization of Papillary Thyroid CarcinomaCell, 2014
- Variants in the ATM‐CHEK2‐BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinomaGenes, Chromosomes and Cancer, 2014
- Response to DNA damage of CHEK2 missense mutations in familial breast cancerHuman Molecular Genetics, 2012
- Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?European Journal of Human Genetics, 2006
- Rare Germ Line CHEK2 Variants Identified in Breast Cancer Families Encode Proteins That Show Impaired ActivationCancer Research, 2006
- CHEK2 Is a Multiorgan Cancer Susceptibility GeneThe American Journal of Human Genetics, 2004