Found: 8
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Prevalence of Homologous Recombination Deficiency Among Patients With Germline RAD51C/D Breast or Ovarian Cancer.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 1, p. e247811, doi. 10.1001/jamanetworkopen.2024.7811
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- Publication type:
- Article
Investigating the effect of 28 BRCA1 and BRCA2 mutations on their related transcribed mRNA.
- Published in:
- Breast Cancer Research & Treatment, 2016, v. 155, n. 2, p. 253, doi. 10.1007/s10549-015-3676-9
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- Publication type:
- Article
Genomically matched therapy in refractory colorectal cancer according to ESMO Scale for Clinical Actionability of Molecular Targets: experience of a comprehensive cancer centre network.
- Published in:
- Molecular Oncology, 2023, v. 17, n. 9, p. 1908, doi. 10.1002/1878-0261.13444
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- Publication type:
- Article
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria.
- Published in:
- Familial Cancer, 2017, v. 16, n. 4, p. 501, doi. 10.1007/s10689-017-9981-1
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- Publication type:
- Article
BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 505, doi. 10.1007/s10689-015-9814-z
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- Publication type:
- Article
Correction: Dueñas et al. Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers 2020, 12 , 3419.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals.
- Published in:
- Cancers, 2020, v. 12, n. 11, p. 3419, doi. 10.3390/cancers12113419
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- Publication type:
- Article
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients.
- Published in:
- Cancers, 2020, v. 12, n. 4, p. 829, doi. 10.3390/cancers12040829
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- Publication type:
- Article