| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An analysis of the efficacy of serial screening for familial nasopharyngeal carcinoma based on Markov chain models
|
Choi, Cheuk Wai
|
|
2010
|
10 |
1 |
p. 133-139
|
artikel
|
| 2 |
A new mutation of BRCA2 gene in an Italian healthy woman with familial breast cancer history
|
Pisanò, Maurizio
|
|
2010
|
10 |
1 |
p. 65-71
|
artikel
|
| 3 |
An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations
|
Ratnayake, Paboda
|
|
2010
|
10 |
1 |
p. 97-105
|
artikel
|
| 4 |
An intronic mutation in MLH1 associated with familial colon and breast cancer
|
Bianchi, F.
|
|
2010
|
10 |
1 |
p. 27-35
|
artikel
|
| 5 |
Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis
|
Win, Aung Ko
|
|
2010
|
10 |
1 |
p. 1-9
|
artikel
|
| 6 |
A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relatives
|
Vos, Joël
|
|
2010
|
10 |
1 |
p. 87-96
|
artikel
|
| 7 |
Cancer survivors: familial risk perception and management advice given to their relatives
|
Eisinger, Francois
|
|
2010
|
10 |
1 |
p. 147-155
|
artikel
|
| 8 |
Care for patients with multiple endocrine neoplasia type 1: the current evidence base
|
Pieterman, C. R. C.
|
|
2010
|
10 |
1 |
p. 157-171
|
artikel
|
| 9 |
Colorectal cancer: no longer the issue in familial adenomatous polyposis?
|
Gibbons, Daniel C.
|
|
2010
|
10 |
1 |
p. 11-20
|
artikel
|
| 10 |
Gene expression in response to ionizing radiation and family history of gastric cancer
|
Marcon, Francesca
|
|
2010
|
10 |
1 |
p. 107-118
|
artikel
|
| 11 |
Genetic epidemiological analysis reveals a multi-gene additive model for gastric cancer
|
Gao, Sanyou
|
|
2010
|
10 |
1 |
p. 119-125
|
artikel
|
| 12 |
Hereditary prostate cancer as a feature of Lynch Syndrome
|
Bauer, Christina M.
|
|
2010
|
10 |
1 |
p. 37-42
|
artikel
|
| 13 |
Identification of a large rearrangement in CYLD as a cause of familial cylindromatosis
|
Ouweland, Ans M. W. van den
|
|
2010
|
10 |
1 |
p. 127-132
|
artikel
|
| 14 |
Inherited germline TP53 mutation encodes a protein with an aberrant C-terminal motif in a case of pediatric adrenocortical tumor
|
Pinto, Emilia M.
|
|
2010
|
10 |
1 |
p. 141-146
|
artikel
|
| 15 |
Mutation analysis of the APC gene in unrelated Korean patients with FAP: four novel mutations with unusual phenotype
|
Han, Sung-Hee
|
|
2010
|
10 |
1 |
p. 21-26
|
artikel
|
| 16 |
Sharing genetic risk with next generation: mutation-positive parents’ communication with their offspring in Lynch Syndrome
|
Aktan-Collan, Katja I.
|
|
2010
|
10 |
1 |
p. 43-50
|
artikel
|
| 17 |
Shortened time interval between colorectal cancer diagnosis and risk testing for hereditary colorectal cancer is not related to higher psychological distress
|
Landsbergen, K. M.
|
|
2010
|
10 |
1 |
p. 51-57
|
artikel
|
| 18 |
Strictly defined familial male breast cancer
|
Güth, Uwe
|
|
2010
|
10 |
1 |
p. 73-77
|
artikel
|
| 19 |
Two BRCA1/2 founder mutations in Jews of Sephardic origin
|
Sagi, Michal
|
|
2010
|
10 |
1 |
p. 59-63
|
artikel
|
| 20 |
What I wish I’d known before surgery: BRCA carriers’ perspectives after bilateral salipingo-oophorectomy
|
Campfield Bonadies, Danielle
|
|
2010
|
10 |
1 |
p. 79-85
|
artikel
|
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