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 |