| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A risk of digestive tract neoplasms susceptibility in miR-146a and miR-196a2
|
Xie, Mingkun
|
|
2014
|
14 |
2 |
p. 229-239
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 5 |
Erratum to: Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers
|
Wei, Chongjuan
|
|
2015
|
14 |
2 |
p. 307
|
article
|
| 6 |
Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer
|
Donner, Iikki
|
|
2015
|
14 |
2 |
p. 241-246
|
article
|
| 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
|
article
|
| 8 |
Germline RAD51B truncating mutation in a family with cutaneous melanoma
|
Wadt, Karin A. W.
|
|
2015
|
14 |
2 |
p. 337-340
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 13 |
Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers
|
Wei, Chongjuan
|
|
2015
|
14 |
2 |
p. 297-306
|
article
|
| 14 |
Parental age and Neurofibromatosis Type 1: a report from the NF1 Patient Registry Initiative
|
Liu, Qian
|
|
2014
|
14 |
2 |
p. 317-324
|
article
|
| 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
|
article
|
| 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
|
article
|
| 17 |
The roles of AXIN2 in tumorigenesis and epigenetic regulation
|
Li, Shuang
|
|
2014
|
14 |
2 |
p. 325-331
|
article
|
Journal description