nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A risk of digestive tract neoplasms susceptibility in miR-146a and miR-196a2
|
Xie, Mingkun |
|
2014 |
14 |
2 |
p. 229-239 |
artikel |
2 |
Comparison of proctocolectomy and ileal pouch-anal anastomosis to colectomy and ileorectal anastomosis in familial adenomatous polyposis
|
Koskenvuo, L. |
|
2014 |
14 |
2 |
p. 221-227 |
artikel |
3 |
Defective DNA mismatch repair activity is common in sebaceous neoplasms, and may be an ineffective approach to screen for Lynch syndrome
|
Lamba, Anu R. |
|
2015 |
14 |
2 |
p. 259-264 |
artikel |
4 |
Desmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis
|
Campos, Fábio Guilherme |
|
2014 |
14 |
2 |
p. 211-219 |
artikel |
5 |
Erratum to: Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers
|
Wei, Chongjuan |
|
2015 |
14 |
2 |
p. 307 |
artikel |
6 |
Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer
|
Donner, Iikki |
|
2015 |
14 |
2 |
p. 241-246 |
artikel |
7 |
First-Line sunitinib in patients with renal cell carcinoma (RCC) in von Hippel–Lindau (VHL) disease: clinical outcome and patterns of radiological response
|
Roma, Anna |
|
2014 |
14 |
2 |
p. 309-316 |
artikel |
8 |
Germline RAD51B truncating mutation in a family with cutaneous melanoma
|
Wadt, Karin A. W. |
|
2015 |
14 |
2 |
p. 337-340 |
artikel |
9 |
Health professionals’ evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer
|
Douma, Kirsten F. L. |
|
2014 |
14 |
2 |
p. 265-272 |
artikel |
10 |
High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations
|
Out, Astrid A. |
|
2015 |
14 |
2 |
p. 247-257 |
artikel |
11 |
Impact of BRCA1/2 mutation on young women’s 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort)
|
Mancini, Julien |
|
2014 |
14 |
2 |
p. 273-279 |
artikel |
12 |
Large genomic rearrangements in the familial breast and ovarian cancer gene BRCA1 are associated with an increased frequency of high risk features
|
James, Paul A. |
|
2015 |
14 |
2 |
p. 287-295 |
artikel |
13 |
Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers
|
Wei, Chongjuan |
|
2015 |
14 |
2 |
p. 297-306 |
artikel |
14 |
Parental age and Neurofibromatosis Type 1: a report from the NF1 Patient Registry Initiative
|
Liu, Qian |
|
2014 |
14 |
2 |
p. 317-324 |
artikel |
15 |
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers
|
Fitarelli-Kiehl, Mariana |
|
2015 |
14 |
2 |
p. 333-336 |
artikel |
16 |
The effect of oral 3,3′-diindolylmethane supplementation on the 2:16α-OHE ratio in BRCA1 mutation carriers
|
Nikitina, Dina |
|
2015 |
14 |
2 |
p. 281-286 |
artikel |
17 |
The roles of AXIN2 in tumorigenesis and epigenetic regulation
|
Li, Shuang |
|
2014 |
14 |
2 |
p. 325-331 |
artikel |