| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer
|
Bielinska, Beata
|
|
2013
|
12 |
4 |
p. 691-698
|
artikel
|
| 2 |
Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes
|
Sie, Aisha S.
|
|
2013
|
12 |
4 |
p. 675-682
|
artikel
|
| 3 |
Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient
|
Butel-Simoes, G. I.
|
|
2013
|
12 |
4 |
p. 647-649
|
artikel
|
| 4 |
Chemoprevention in Lynch syndrome
|
Burn, John
|
|
2013
|
12 |
4 |
p. 707-718
|
artikel
|
| 5 |
Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer?
|
Bronner, Karen
|
|
2013
|
12 |
4 |
p. 629-637
|
artikel
|
| 6 |
Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives
|
Hazewinkel, Yark
|
|
2013
|
12 |
4 |
p. 669-673
|
artikel
|
| 7 |
Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutation
|
Kim, Dongwon
|
|
2013
|
12 |
4 |
p. 621-628
|
artikel
|
| 8 |
Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome
|
Fujii, Katsunori
|
|
2013
|
12 |
4 |
p. 611-614
|
artikel
|
| 9 |
“High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis”
|
Alderlieste, Yasser A.
|
|
2013
|
12 |
4 |
p. 699-706
|
artikel
|
| 10 |
Interest of individuals from BRCA families to participate in research studies focused on male BRCA carriers
|
Pal, Tuya
|
|
2013
|
12 |
4 |
p. 615-619
|
artikel
|
| 11 |
Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?
|
Lapointe, Julie
|
|
2013
|
12 |
4 |
p. 601-610
|
artikel
|
| 12 |
Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity
|
Farrell, M. P.
|
|
2013
|
12 |
4 |
p. 741-747
|
artikel
|
| 13 |
Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence
|
Juan Jiménez, Inmaculada de
|
|
2013
|
12 |
4 |
p. 767-777
|
artikel
|
| 14 |
Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry
|
Casey, Murray Joseph
|
|
2013
|
12 |
4 |
p. 719-740
|
artikel
|
| 15 |
Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer
|
Li, Shuying
|
|
2013
|
12 |
4 |
p. 755-765
|
artikel
|
| 16 |
Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer
|
Alanee, Shaheen
|
|
2013
|
12 |
4 |
p. 597-600
|
artikel
|
| 17 |
Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study
|
Aktan-Collan, Katja
|
|
2013
|
12 |
4 |
p. 639-646
|
artikel
|
| 18 |
Rectal cancers in patients with familial adenomatous polyposis
|
Liang, Jennifer
|
|
2013
|
12 |
4 |
p. 749-754
|
artikel
|
| 19 |
Self administered screening for hereditary cancers in conjunction with mammography and ultrasound
|
McDonnell, Charles H.
|
|
2013
|
12 |
4 |
p. 651-656
|
artikel
|
| 20 |
The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia
|
Teo, Zhi L.
|
|
2013
|
12 |
4 |
p. 587-595
|
artikel
|
| 21 |
The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012
|
|
|
2013
|
12 |
4 |
p. 779-809
|
artikel
|
| 22 |
Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients
|
Plakhins, Grigorijs
|
|
2013
|
12 |
4 |
p. 683-689
|
artikel
|
| 23 |
Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia
|
Zhu, Jie
|
|
2013
|
12 |
4 |
p. 657-667
|
artikel
|
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