| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A randomized controlled trial of diet and physical activity in BRCA mutation carriers
|
Pasanisi, P.
|
|
2013
|
13 |
2 |
p. 181-187
|
artikel
|
| 2 |
Attitudes and knowledge of medical practitioners to hereditary cancer clinics and cancer genetic testing
|
Teng, Ian
|
|
2013
|
13 |
2 |
p. 311-324
|
artikel
|
| 3 |
Barrett’s esophagus in the patients with familial adenomatous polyposis
|
Gatalica, Zoran
|
|
2013
|
13 |
2 |
p. 213-217
|
artikel
|
| 4 |
Baseline and post prophylactic tubal–ovarian surgery CA125 levels in BRCA1 and BRCA2 mutation carriers
|
Chen, Ying
|
|
2014
|
13 |
2 |
p. 197-203
|
artikel
|
| 5 |
Breast cancer risk assessment in 8,824 women attending a family history evaluation and screening programme
|
Evans, D. Gareth R.
|
|
2013
|
13 |
2 |
p. 189-196
|
artikel
|
| 6 |
Capsule endoscopy versus magnetic resonance enterography for the detection of small bowel polyps in Peutz–Jeghers syndrome
|
Urquhart, P.
|
|
2014
|
13 |
2 |
p. 249-255
|
artikel
|
| 7 |
Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes
|
Rich, Thereasa A.
|
|
2013
|
13 |
2 |
p. 291-299
|
artikel
|
| 8 |
Deletion of exons 1–3 of the MEN1 gene in a large Italian family causes the loss of menin expression
|
Zatelli, Maria Chiara
|
|
2014
|
13 |
2 |
p. 273-280
|
artikel
|
| 9 |
Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation
|
Hasani-Ranjbar, Shirin
|
|
2013
|
13 |
2 |
p. 267-272
|
artikel
|
| 10 |
Evaluation after five years of the cancer genetic counselling programme of Valencian Community (Eastern Spain)
|
Cuevas-Cuerda, Dolores
|
|
2013
|
13 |
2 |
p. 301-309
|
artikel
|
| 11 |
Impact of familial risk and mammography screening on prognostic indicators of breast disease among women from the Ontario site of the Breast Cancer Family Registry
|
Walker, Meghan J.
|
|
2013
|
13 |
2 |
p. 163-172
|
artikel
|
| 12 |
Inversion of exons 1–7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population
|
Rhees, Jennifer
|
|
2013
|
13 |
2 |
p. 219-225
|
artikel
|
| 13 |
Is intraductal tubulopapillary neoplasia a new entity in the spectrum of familial pancreatic cancer syndrome?
|
Chiaro, Marco Del
|
|
2013
|
13 |
2 |
p. 227-229
|
artikel
|
| 14 |
Large genomic rearrangement of BRCA1 and BRCA2 genes in familial breast cancer patients in Korea
|
Cho, Ja Young
|
|
2014
|
13 |
2 |
p. 205-211
|
artikel
|
| 15 |
Misperceptions of ovarian cancer risk in women at increased risk for hereditary ovarian cancer
|
Meiser, Bettina
|
|
2013
|
13 |
2 |
p. 153-162
|
artikel
|
| 16 |
More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling
|
Sie, Aisha S.
|
|
2013
|
13 |
2 |
p. 143-151
|
artikel
|
| 17 |
Potential genetic anticipation in hereditary leiomyomatosis-renal cell cancer (HLRCC)
|
Wong, Mei Hua
|
|
2014
|
13 |
2 |
p. 281-289
|
artikel
|
| 18 |
Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe
|
Noskowicz, Monika
|
|
2013
|
13 |
2 |
p. 137-142
|
artikel
|
| 19 |
Prophylactic total gastrectomy in hereditary diffuse gastric cancer: identification of two novel CDH1 gene mutations—a clinical observational study
|
Bardram, Linda
|
|
2014
|
13 |
2 |
p. 231-242
|
artikel
|
| 20 |
Providing patient education: impact on quantity and quality of family health history collection
|
Beadles, Chris A.
|
|
2014
|
13 |
2 |
p. 325-332
|
artikel
|
| 21 |
RAD51 135G>C and TP53 Arg72Pro polymorphisms and susceptibility to breast cancer in Serbian women
|
Krivokuca, Ana M.
|
|
2013
|
13 |
2 |
p. 173-180
|
artikel
|
| 22 |
Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families
|
Jasperson, Kory W.
|
|
2013
|
13 |
2 |
p. 257-265
|
artikel
|
| 23 |
The MUTYH hotspot mutations p.G396D and p.Y179C do not cause substantial genetic susceptibility to biliary cancer
|
Casper, M.
|
|
2014
|
13 |
2 |
p. 243-247
|
artikel
|
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