| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
|
Jenkins, Mark A.
|
|
2019
|
18 |
4 |
p. 389-397
|
artikel
|
| 2 |
Assessing a single SNP located at TERT/CLPTM1L multi-cancer risk region as a genetic modifier for risk of pancreatic cancer and melanoma in Dutch CDKN2A mutation carriers
|
Christodoulou, E.
|
|
2019
|
18 |
4 |
p. 439-444
|
artikel
|
| 3 |
Energy balance related lifestyle factors and risk of endometrial and colorectal cancer among individuals with lynch syndrome: a systematic review
|
Coletta, Adriana M.
|
|
2019
|
18 |
4 |
p. 399-420
|
artikel
|
| 4 |
Health behaviours and beliefs in individuals with familial pancreatic cancer
|
Underhill-Blazey, Meghan
|
|
2019
|
18 |
4 |
p. 457-464
|
artikel
|
| 5 |
Hereditary diffuse gastric cancer: cancer risk and the personal cost of preventive surgery
|
Kaurah, P.
|
|
2019
|
18 |
4 |
p. 429-438
|
artikel
|
| 6 |
Inequities in multi-gene hereditary cancer testing: lower diagnostic yield and higher VUS rate in individuals who identify as Hispanic, African or Asian and Pacific Islander as compared to European
|
Ndugga-Kabuye, Mesaki K.
|
|
2019
|
18 |
4 |
p. 465-469
|
artikel
|
| 7 |
Lynch syndrome with exclusive skin involvement: time to consider a molecular definition?
|
Vaisfeld, Alessandro
|
|
2019
|
18 |
4 |
p. 421-427
|
artikel
|
| 8 |
Multiple primary malignancies associated with a germline SMARCB1 pathogenic variant
|
Eelloo, Judith A.
|
|
2019
|
18 |
4 |
p. 445-449
|
artikel
|
| 9 |
Population frequencies of pathogenic alleles of BRCA1 and BRCA2: analysis of 173 Danish breast cancer pedigrees using the BOADICEA model
|
Terkelsen, Thorkild
|
|
2019
|
18 |
4 |
p. 381-388
|
artikel
|
| 10 |
Should unaffected female BRCA2 pathogenic variant carriers be told there is little or no advantage from risk reducing mastectomy?
|
Evans, D. Gareth
|
|
2019
|
18 |
4 |
p. 377-379
|
artikel
|
| 11 |
TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling
|
Bittar, Camila Matzenbacher
|
|
2019
|
18 |
4 |
p. 451-456
|
artikel
|
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