nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Analysis of PALB2 in a cohort of Italian breast cancer patients: identification of a novel PALB2 truncating mutation
|
Vietri, Maria Teresa |
|
2015 |
14 |
3 |
p. 341-348 |
artikel |
2 |
A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine
|
Hansen, Maren F. |
|
2015 |
14 |
3 |
p. 437-448 |
artikel |
3 |
Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome
|
Cruz-Correa, Marcia |
|
2015 |
14 |
3 |
p. 415-425 |
artikel |
4 |
Genetic screening in patients with Retinoblastoma in Israel
|
Sagi, Michal |
|
2015 |
14 |
3 |
p. 471-480 |
artikel |
5 |
Germline mutations predisposing to non-small cell lung cancer
|
Clamon, Gerald H. |
|
2015 |
14 |
3 |
p. 463-469 |
artikel |
6 |
Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation
|
Kim, Haeyoung |
|
2015 |
14 |
3 |
p. 365-371 |
artikel |
7 |
Implementing a telephone based peer support intervention for women with a BRCA1/2 mutation
|
Farrelly, Ashley |
|
2015 |
14 |
3 |
p. 373-382 |
artikel |
8 |
Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews
|
Rosner, Guy |
|
2015 |
14 |
3 |
p. 427-436 |
artikel |
9 |
Pitfalls in the diagnosis of biallelic PMS2 mutations
|
Antelo, Marina |
|
2015 |
14 |
3 |
p. 411-414 |
artikel |
10 |
Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican population
|
Macías-Gómez, Nelly M. |
|
2015 |
14 |
3 |
p. 349-354 |
artikel |
11 |
Risk factors for endometrial cancer among women with a BRCA1 or BRCA2 mutation: a case control study
|
Segev, Yakir |
|
2015 |
14 |
3 |
p. 383-391 |
artikel |
12 |
Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz–Jeghers syndrome
|
Borun, Pawel |
|
2015 |
14 |
3 |
p. 455-461 |
artikel |
13 |
The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24
|
Rudkjøbing, Laura Aviaja |
|
2015 |
14 |
3 |
p. 393-400 |
artikel |
14 |
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
|
Varga, Elizabeth |
|
2015 |
14 |
3 |
p. 481-485 |
artikel |
15 |
Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study
|
Wevers, M. R. |
|
2015 |
14 |
3 |
p. 355-363 |
artikel |
16 |
3′-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity
|
Kondelin, Johanna |
|
2015 |
14 |
3 |
p. 449-453 |
artikel |
17 |
Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer
|
Kallenberg, F. G. J. |
|
2015 |
14 |
3 |
p. 401-410 |
artikel |
18 |
Zebrafish xenotransplantation as a tool for in vivo cancer study
|
Zhang, Beibei |
|
2015 |
14 |
3 |
p. 487-493 |
artikel |