Found: 8
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Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing.
- Published in:
- 2018
- By:
- Publication type:
- journal article
High risk of breast cancer in women with biallelic pathogenic variants in CHEK2.
- Published in:
- Breast Cancer Research & Treatment, 2020, v. 180, n. 2, p. 503, doi. 10.1007/s10549-020-05543-3
- By:
- Publication type:
- Article
Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA Analysis.
- Published in:
- Familial Cancer, 2022, v. 21, n. 1, p. 7, doi. 10.1007/s10689-020-00224-y
- By:
- Publication type:
- Article
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry.
- Published in:
- Familial Cancer, 2014, v. 13, n. 4, p. 573, doi. 10.1007/s10689-014-9744-1
- By:
- Publication type:
- Article
In Reply.
- Published in:
- Oncologist, 2017, v. 22, n. 12, p. 1540, doi. 10.1634/theoncologist.2017-0320
- By:
- Publication type:
- Article
Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory.
- Published in:
- Oncologist, 2017, v. 22, n. 7, p. 797, doi. 10.1634/theoncologist.2016-0431
- By:
- Publication type:
- Article
Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome.
- Published in:
- Frontiers in Oncology, 2023, v. 13, p. 1, doi. 10.3389/fonc.2023.1069467
- By:
- Publication type:
- Article
Update on pediatric cancer predisposition syndromes.
- Published in:
- Pediatric Blood & Cancer, 2013, v. 60, n. 8, p. 1247, doi. 10.1002/pbc.24555
- By:
- Publication type:
- Article