| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A pre-visit tailored website enhances counselees’ realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling
|
Albada, Akke
|
|
2011
|
11 |
1 |
p. 85-95
|
artikel
|
| 2 |
A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours
|
Schofield, Lyn
|
|
2011
|
11 |
1 |
p. 1-6
|
artikel
|
| 3 |
BRCA1 and BRCA2 germline mutations in 85 Iranian breast cancer patients
|
Keshavarzi, Fatemeh
|
|
2011
|
11 |
1 |
p. 57-67
|
artikel
|
| 4 |
Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma
|
Qi, X.-P.
|
|
2011
|
11 |
1 |
p. 131-136
|
artikel
|
| 5 |
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy
|
Ghiorzo, P.
|
|
2011
|
11 |
1 |
p. 41-47
|
artikel
|
| 6 |
Evaluation of the BOADICEA risk assessment model in women with a family history of breast cancer
|
Ståhlbom, Anne Kinhult
|
|
2011
|
11 |
1 |
p. 33-40
|
artikel
|
| 7 |
Familial renal cancer as an indicator of hereditary leiomyomatosis and renal cell cancer syndrome
|
Raymond, Victoria M.
|
|
2011
|
11 |
1 |
p. 115-121
|
artikel
|
| 8 |
First degree relatives and familial aggregation of gastric cancer: who to choose for control in case–control studies?
|
Marcos-Pinto, Ricardo
|
|
2011
|
11 |
1 |
p. 137-143
|
artikel
|
| 9 |
Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance
|
Spaendonck-Zwarts, Karin Y. van
|
|
2011
|
11 |
1 |
p. 123-129
|
artikel
|
| 10 |
Implications for cancer genetics practice of pro-actively assessing family history in a General Practice cohort in North West London
|
Kohut, Kelly
|
|
2011
|
11 |
1 |
p. 107-113
|
artikel
|
| 11 |
Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients
|
Magnusson, Susanne
|
|
2011
|
11 |
1 |
p. 145-155
|
artikel
|
| 12 |
Low prevalence of BRCA1 and BRCA2 mutations in the sporadic breast cancer of Spanish population
|
Juan Jiménez, Inmaculada de
|
|
2011
|
11 |
1 |
p. 49-56
|
artikel
|
| 13 |
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
|
Rahner, Nils
|
|
2011
|
11 |
1 |
p. 19-26
|
artikel
|
| 14 |
Non-cancer endpoints in BRCA1/2 carriers after risk-reducing salpingo-oophorectomy
|
Cohen, J. V.
|
|
2011
|
11 |
1 |
p. 69-75
|
artikel
|
| 15 |
Patient outcomes associated with group and individual genetic counseling formats
|
Rothwell, Erin
|
|
2011
|
11 |
1 |
p. 97-106
|
artikel
|
| 16 |
Self-reported mammography use following BRCA1/2 genetic testing may be overestimated
|
Larouche, Geneviève
|
|
2011
|
11 |
1 |
p. 27-32
|
artikel
|
| 17 |
The liver: another organ involved in Muir Torre syndrome?
|
Morando, F.
|
|
2011
|
11 |
1 |
p. 7-12
|
artikel
|
| 18 |
Two novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients
|
Shahmoradi, Somayeh
|
|
2011
|
11 |
1 |
p. 13-17
|
artikel
|
| 19 |
Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/2 mutations carriers: the LIBER trial
|
Pujol, Pascal
|
|
2011
|
11 |
1 |
p. 77-84
|
artikel
|
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