Works matching IS 13899600 AND DT 2015 AND VI 14 AND IP 3
Results: 18
Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican population.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 349, doi. 10.1007/s10689-015-9787-y
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- Publication type:
- Article
Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 355, doi. 10.1007/s10689-015-9788-x
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- Publication type:
- Article
Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 365, doi. 10.1007/s10689-015-9789-9
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- Publication type:
- Article
The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an MLH1 variant of uncertain significance.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 481, doi. 10.1007/s10689-015-9790-3
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- Publication type:
- Article
The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 393, doi. 10.1007/s10689-015-9791-2
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- Publication type:
- Article
Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 401, doi. 10.1007/s10689-015-9792-1
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- Publication type:
- Article
Pitfalls in the diagnosis of biallelic PMS2 mutations.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 411, doi. 10.1007/s10689-015-9793-0
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- Publication type:
- Article
Genetic screening in patients with Retinoblastoma in Israel.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 471, doi. 10.1007/s10689-015-9794-z
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- Publication type:
- Article
Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 415, doi. 10.1007/s10689-015-9795-y
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- Publication type:
- Article
Germline mutations predisposing to non-small cell lung cancer.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 463, doi. 10.1007/s10689-015-9796-x
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- Publication type:
- Article
Implementing a telephone based peer support intervention for women with a BRCA1/2 mutation.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 373, doi. 10.1007/s10689-015-9797-9
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- Publication type:
- Article
Risk factors for endometrial cancer among women with a BRCA1 or BRCA2 mutation: a case control study.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 383, doi. 10.1007/s10689-015-9798-8
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- Publication type:
- Article
Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 427, doi. 10.1007/s10689-015-9799-7
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- Publication type:
- Article
Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 455, doi. 10.1007/s10689-015-9800-5
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- Publication type:
- Article
Zebrafish xenotransplantation as a tool for in vivo cancer study.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 487, doi. 10.1007/s10689-015-9802-3
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- Publication type:
- Article
A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 437, doi. 10.1007/s10689-015-9803-2
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- Publication type:
- Article
3′-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity.
- Published in:
- Familial Cancer, 2015, v. 14, n. 3, p. 449, doi. 10.1007/s10689-015-9804-1
- By:
- Publication type:
- Article
Analysis of PALB2 in a cohort of Italian breast cancer patients: identification of a novel PALB2 truncating mutation.
- Published in:
- 2015
- By:
- Publication type:
- Letter