| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A functional HOTAIR rs920778 polymorphism does not contributes to gastric cancer in a Turkish population: a case–control study
|
Bayram, Süleyman
|
|
2015
|
14 |
4 |
p. 561-567
|
artikel
|
| 2 |
Birt–Hogg–Dubé syndrome and intracranial vascular pathologies
|
Kapoor, Rahul
|
|
2015
|
14 |
4 |
p. 595-597
|
artikel
|
| 3 |
BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study
|
de Juan, Inmaculada
|
|
2015
|
14 |
4 |
p. 505-513
|
artikel
|
| 4 |
BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review
|
Spinelli, Claudio
|
|
2015
|
14 |
4 |
p. 515-519
|
artikel
|
| 5 |
Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines
|
Marcus, Rebecca K.
|
|
2015
|
14 |
4 |
p. 641-649
|
artikel
|
| 6 |
Childhood cancers in families with and without Lynch syndrome
|
Heath, John A.
|
|
2015
|
14 |
4 |
p. 545-551
|
artikel
|
| 7 |
Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis
|
Bugalho, Maria João
|
|
2015
|
14 |
4 |
p. 603-607
|
artikel
|
| 8 |
Follicular variant of papillary thyroid cancer in Alström syndrome
|
Papadakis, M.
|
|
2015
|
14 |
4 |
p. 599-602
|
artikel
|
| 9 |
Genotype–phenotype analysis of von Hippel–Lindau syndrome in fifteen Indian families
|
Vikkath, Narendranath
|
|
2015
|
14 |
4 |
p. 585-594
|
artikel
|
| 10 |
High accuracy of family history of melanoma in Danish melanoma cases
|
Wadt, Karin A. W.
|
|
2015
|
14 |
4 |
p. 609-613
|
artikel
|
| 11 |
Massive gastric polyposis associated with a germline SMAD4 gene mutation
|
Soer, Eline
|
|
2015
|
14 |
4 |
p. 569-573
|
artikel
|
| 12 |
Metastatic sympathetic paraganglioma in a patient with loss of the SDHC gene
|
Rich, Thereasa
|
|
2015
|
14 |
4 |
p. 615-619
|
artikel
|
| 13 |
POLE mutations in families predisposed to cutaneous melanoma
|
Aoude, Lauren G.
|
|
2015
|
14 |
4 |
p. 621-628
|
artikel
|
| 14 |
Prevalence and detection of psychosocial problems in cancer genetic counseling
|
Eijzenga, W.
|
|
2015
|
14 |
4 |
p. 629-636
|
artikel
|
| 15 |
Psychological distress related to BRCA testing in ovarian cancer patients
|
Bjørnslett, Merete
|
|
2015
|
14 |
4 |
p. 495-504
|
artikel
|
| 16 |
Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene
|
Win, Aung Ko
|
|
2015
|
14 |
4 |
p. 575-583
|
artikel
|
| 17 |
Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis
|
Basu, N. N.
|
|
2015
|
14 |
4 |
p. 531-538
|
artikel
|
| 18 |
Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK
|
Chandrasekaran, Dhivya
|
|
2015
|
14 |
4 |
p. 521-530
|
artikel
|
| 19 |
Supporting families with Cancer: A patient centred survivorship model of care
|
Craft, Emily Victoria
|
|
2015
|
14 |
4 |
p. 637-640
|
artikel
|
| 20 |
Survival in familial colorectal cancer: a Danish cohort study
|
Lautrup, Charlotte Kvist
|
|
2015
|
14 |
4 |
p. 553-559
|
artikel
|
| 21 |
The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy
|
Aa, Jessica E. van der
|
|
2015
|
14 |
4 |
p. 539-544
|
artikel
|
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