Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             17 gevonden resultaten
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
                             17 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland