Found: 9
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BRCA1 founder mutations and beyond in the Polish population: A single-institution BRCA1/2 next-generation sequencing study.
- Published in:
- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0201086
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- Publication type:
- Article
The impact of oophorectomy on survival from breast cancer in patients with CHEK2 mutations.
- Published in:
- 2022
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- Publication type:
- journal article
SOMATIC MUTATIONS IN BRCA1 AND 2 IN 201 UNSELECTED OVARIAN CARCINOMA SAMPLES -SINGLE INSTITUTION STUDY.
- Published in:
- Polish Journal of Pathology: Official Journal of the Polish Society of Pathologists, 2019, v. 70, n. 2, p. 115, doi. 10.5114/pjp.2019.82905
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- Publication type:
- Article
High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-58
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- Publication type:
- Article
Relationship between the Expression of CHK2 and p53 in Tumor Tissue and the Course of Papillary Thyroid Cancer in Patients with CHEK2 Germline Mutations.
- Published in:
- Cancers, 2024, v. 16, n. 4, p. 815, doi. 10.3390/cancers16040815
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- Publication type:
- Article
Incidence of the CHEK2 Germline Mutation and Its Impact on Clinicopathological Features, Treatment Responses, and Disease Course in Patients with Papillary Thyroid Carcinoma.
- Published in:
- Cancers, 2021, v. 13, n. 3, p. 470, doi. 10.3390/cancers13030470
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- Publication type:
- Article
Coexisting Germline CHEK2 and Somatic BRAFV600E Mutations in Papillary Thyroid Cancer and Their Association with Clinicopathological Features and Disease Course.
- Published in:
- Cancers, 2019, v. 11, n. 11, p. 1744, doi. 10.3390/cancers11111744
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- Publication type:
- Article
CHEK 2 mutations and the risk of papillary thyroid cancer.
- Published in:
- International Journal of Cancer, 2015, v. 137, n. 3, p. 548, doi. 10.1002/ijc.29426
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- Publication type:
- Article
Screening with magnetic resonance imaging, mammography and ultrasound in women at average and intermediate risk of breast cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0064-y
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- Publication type:
- Article