Last Posted: Dec 28, 2020
- [Hereditary cancer syndromes: a modern paradigm].
Baranova Elena E et al. Problemy endokrinologii 2020 Sep 66(4) 24-34 - A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer Patients.
Feliubadaló Lidia et al. Clinical chemistry 2020 Dec - Mastermind: A Comprehensive Genomic Association Search Engine for Empirical Evidence Curation and Genetic Variant Interpretation.
Chunn Lauren M et al. Frontiers in genetics 2020 11577152 - NCCN Updates Guidelines for Hereditary Cancer Risks.
et al. American journal of medical genetics. Part A 2020 Dec 182(12) 2813-2814 - New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients.
Djursby Malene et al. Frontiers in genetics 2020 11566266 - How to structure an oncogenetics service for the public health system: Report of the implementation of the first service in Northeastern Brazil.
Nogueira Camila Sampaio et al. Cancer genetics 2020 Nov 250-2516-11 - Spectrum of mutations in genes associated with familial colorectal cancer syndrome (MLH1, MSH2, PMS2, MSH6, and APC): A not so common hereditary cancer syndrome in Indian population.
Bhai Pratibha et al. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2020 Nov - Health Care Disparities and Demand for Expanding Hereditary Breast Cancer Screening Guidelines in African Americans.
Ciuro Jordan et al. Clinical breast cancer 2020 Sep - Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets.
Berger Mark J et al. Database : the journal of biological databases and curation 2020 Jan 2020 - Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility.
Tudini Emma et al. Journal of medical genetics 2020 Nov
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