Clinical and molecular markers guide the genetics of pheochromocytoma and paraganglioma
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Publisher
Elsevier BV
Reference51 articles.
1. Genetic bases of pheochromocytoma and paraganglioma;Cascon;J. Mol. Endocrinol.,2023
2. Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing;Fishbein;Ann. Surg. Oncol.,2013
3. Consensus statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas;Group NGSiPS;Nat. Rev. Endocrinol.,2017
4. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology;Richards;Genet. Med.,2015
5. Novel DNMT3A germline variant in a patient with multiple Paragangliomas and papillary thyroid carcinoma;Mellid;Cancers (Basel),2020
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