| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery
|
Shapira, Rachel
|
|
2017
|
17 |
4 |
p. 485-493
|
artikel
|
| 2 |
APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis
|
Stormorken, Astrid Tenden
|
|
2018
|
17 |
4 |
p. 539-543
|
artikel
|
| 3 |
A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC)
|
Bhola, Priya T.
|
|
2018
|
17 |
4 |
p. 615-620
|
artikel
|
| 4 |
Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate risk
|
West, Allison H.
|
|
2018
|
17 |
4 |
p. 495-505
|
artikel
|
| 5 |
Commentary: PREMM5 threshold of 2.5% is recommended to improve identification of PMS2 carriers
|
Kastrinos, Fay
|
|
2018
|
17 |
4 |
p. 567
|
artikel
|
| 6 |
Correlation of IL-31 gene polymorphisms with susceptibility and clinical recurrence of bladder cancer
|
Li, Qin
|
|
2017
|
17 |
4 |
p. 577-585
|
artikel
|
| 7 |
Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline
|
Kanga-Parabia, Anaita
|
|
2018
|
17 |
4 |
p. 547-555
|
artikel
|
| 8 |
Feasibility of endoscopic resection using bipolar snare for nonampullary duodenal tumours in familial adenomatous polyposis patients
|
Inoki, Kazuya
|
|
2017
|
17 |
4 |
p. 517-524
|
artikel
|
| 9 |
Gene expression analysis in peripheral blood cells of patients with hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC): identification of NRF2 pathway activation
|
Arenas Valencia, Carolina
|
|
2018
|
17 |
4 |
p. 587-599
|
artikel
|
| 10 |
Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation
|
Salomé, Jenny von
|
|
2017
|
17 |
4 |
p. 531-537
|
artikel
|
| 11 |
Letter to the editor
|
Anele, C. C.
|
|
2018
|
17 |
4 |
p. 565-566
|
artikel
|
| 12 |
Metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis
|
Malik, Salim S.
|
|
2017
|
17 |
4 |
p. 557-564
|
artikel
|
| 13 |
Molecular analysis of an asbestos-exposed Belgian family with a high prevalence of mesothelioma
|
Hylebos, Marieke
|
|
2018
|
17 |
4 |
p. 569-576
|
artikel
|
| 14 |
Mutations in context: implications of BRCA testing in diverse populations
|
Felix, Gabriela E. S.
|
|
2017
|
17 |
4 |
p. 471-483
|
artikel
|
| 15 |
Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same
|
Huq, A. J.
|
|
2018
|
17 |
4 |
p. 601-606
|
artikel
|
| 16 |
Response to letter to editor regarding published article—metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis
|
Lythgoe, Mark P.
|
|
2018
|
17 |
4 |
p. 545-546
|
artikel
|
| 17 |
Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience
|
Courtney, Eliza
|
|
2018
|
17 |
4 |
p. 621-626
|
artikel
|
| 18 |
SNP association study in PMS2-associated Lynch syndrome
|
Broeke, Sanne W. ten
|
|
2017
|
17 |
4 |
p. 507-515
|
artikel
|
| 19 |
The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome
|
Macaulay, Shelley
|
|
2018
|
17 |
4 |
p. 607-613
|
artikel
|
| 20 |
Urological sequelae of desmoids associated with familial adenomatous polyposis
|
Walton, S. J.
|
|
2018
|
17 |
4 |
p. 525-530
|
artikel
|
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