| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months
|
Zhang, Jin
|
|
2011
|
11 |
2 |
p. 209-214
|
artikel
|
| 2 |
Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening
|
Cozzolino, Angela M.
|
|
2011
|
11 |
2 |
p. 201-208
|
artikel
|
| 3 |
A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney–Stratakis dyad
|
Celestino, Ricardo
|
|
2011
|
11 |
2 |
p. 189-194
|
artikel
|
| 4 |
Can a gastrointestinal pathologist identify microsatellite instability in colorectal cancer with reproducibility and a high degree of specificity?
|
Brazowski, Eli
|
|
2012
|
11 |
2 |
p. 249-257
|
artikel
|
| 5 |
Families’ experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population
|
Mendes, Álvaro
|
|
2012
|
11 |
2 |
p. 291-306
|
artikel
|
| 6 |
French women’s breast self-examination practices with time after undergoing BRCA1/2 genetic testing
|
Maheu, C.
|
|
2012
|
11 |
2 |
p. 269-278
|
artikel
|
| 7 |
Hereditary medullary thyroid carcinoma: the management dilemma
|
Zhou, Ping
|
|
2011
|
11 |
2 |
p. 157-165
|
artikel
|
| 8 |
Looking different, feeling different: women’s reactions to risk-reducing breast and ovarian surgery
|
Hallowell, Nina
|
|
2011
|
11 |
2 |
p. 215-224
|
artikel
|
| 9 |
Management of duodenal adenomatosis in FAP: single centre experience
|
Drini, Musa
|
|
2011
|
11 |
2 |
p. 167-173
|
artikel
|
| 10 |
Predictive genetic testing of first degree relatives of mutation carriers is a cost-effective strategy in preventing hereditary non-polyposis colorectal cancer in Singapore
|
Wang, Vivian Wei
|
|
2012
|
11 |
2 |
p. 279-289
|
artikel
|
| 11 |
Preimplantation genetic diagnosis for inherited breast cancer: first clinical application and live birth in Spain
|
Ramón y Cajal, Teresa
|
|
2011
|
11 |
2 |
p. 175-179
|
artikel
|
| 12 |
Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients
|
Rashid, Muhammad U.
|
|
2012
|
11 |
2 |
p. 307-311
|
artikel
|
| 13 |
Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist’s initiative
|
Landsbergen, K. M.
|
|
2012
|
11 |
2 |
p. 259-267
|
artikel
|
| 14 |
RB1 mutations and second primary malignancies after hereditary retinoblastoma
|
Dommering, Charlotte J.
|
|
2011
|
11 |
2 |
p. 225-233
|
artikel
|
| 15 |
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations
|
Moran, A.
|
|
2011
|
11 |
2 |
p. 235-242
|
artikel
|
| 16 |
The founder Ashkenazi Jewish mutations in the MSH2 and MSH6 genes in Israeli patients with gastric and pancreatic cancer
|
Laitman, Yael
|
|
2012
|
11 |
2 |
p. 243-247
|
artikel
|
| 17 |
Urologists’ and GPs’ knowledge of hereditary prostate cancer is suboptimal for prostate cancer counseling: a nation-wide survey in The Netherlands
|
Cremers, Ruben
|
|
2011
|
11 |
2 |
p. 195-200
|
artikel
|
| 18 |
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families
|
Schneegans, S. M.
|
|
2011
|
11 |
2 |
p. 181-188
|
artikel
|
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