Found: 16
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Only 32.3% of Breast Cancer Families with Pathogenic Variants in Cancer Genes Utilized Cascade Genetic Testing.
- Published in:
- Cancers, 2023, v. 15, n. 21, p. 5218, doi. 10.3390/cancers15215218
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- Publication type:
- Article
Characterization of the c.793-1G > A splicing variant in CHEK2 gene as pathogenic: a case report.
- Published in:
- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0862-3
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- Publication type:
- Article
Gender Specificity of a Genetic Variant of Androgen Receptor and Risk of Coronary Artery Disease.
- Published in:
- 2016
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- Publication type:
- journal article
Germline Co-deletion of CDKN2A and CDKN2B Genes in Pleomorphic Xanthoastrocytoma: Case Report.
- Published in:
- In Vivo, 2024, v. 38, n. 4, p. 1671, doi. 10.21873/invivo.13617
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- Publication type:
- Article
Neuroendocrine Breast Tumors: Could Multigene Assays Help in Guiding Treatment Decisions? Case Presentation.
- Published in:
- In Vivo, 2024, v. 38, n. 3, p. 1443, doi. 10.21873/invivo.13587
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- Publication type:
- Article
Reclassification of Splicing Gene Variants in Hereditary Cancer: Cases Report and Literature Review.
- Published in:
- In Vivo, 2023, v. 37, n. 4, p. 1432, doi. 10.21873/invivo.13227
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- Publication type:
- Article
Report of a germline double heterozygote in MSH2 and PALB2.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1242
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- Publication type:
- Article
Importance of multigene panel test in patients with consanguineous marriage and family history of breast cancer.
- Published in:
- Oncology Letters, 2022, v. 23, n. 4, p. N.PAG, doi. 10.3892/ol.2022.13238
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- Publication type:
- Article
Determination of EGFR and KRAS mutational status in Greek non-small-cell lung cancer patients.
- Published in:
- Oncology Letters, 2015, v. 10, n. 4, p. 2176, doi. 10.3892/ol.2015.3600
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- Publication type:
- Article
The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic Laboratory.
- Published in:
- Cancer Genomics & Proteomics (1109-6535), 2024, v. 21, n. 5, p. 448, doi. 10.21873/cgp.20463
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- Publication type:
- Article
Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer Testing.
- Published in:
- Cancer Genomics & Proteomics (1109-6535), 2023, v. 20, n. 5, p. 448, doi. 10.21873/cgp.20396
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- Publication type:
- Article
Revisiting the Implications of Positive Germline Testing Results Using Multi-gene Panels in Breast Cancer Patients.
- Published in:
- Cancer Genomics & Proteomics (1109-6535), 2022, v. 19, n. 1, p. 60, doi. 10.21873/cgp.20304
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- Publication type:
- Article
Clinical Utility of Functional RNA Analysis for the Reclassification of Splicing Gene Variants in Hereditary Cancer.
- Published in:
- Cancer Genomics & Proteomics (1109-6535), 2021, v. 18, n. 3, p. 285, doi. 10.21873/cgp.20259
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- Publication type:
- Article
Polygenic Risk Score (PRS) Combined with NGS Panel Testing Increases Accuracy in Hereditary Breast Cancer Risk Estimation.
- Published in:
- Diagnostics (2075-4418), 2024, v. 14, n. 16, p. 1826, doi. 10.3390/diagnostics14161826
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- Publication type:
- Article
Genetic variation in the CYP17 gene and recurrent spontaneous abortions.
- Published in:
- 2011
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- Publication type:
- journal article
Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations.
- Published in:
- 2019
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- Publication type:
- journal article