| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene
|
Vernez, M.
|
|
2006
|
6 |
1 |
p. 141-145
|
artikel
|
| 2 |
Acceptance of preventive surgeries by Israeli women who had undergone BRCA testing
|
Kram, Vardit
|
|
2007
|
6 |
1 |
p. 159
|
artikel
|
| 3 |
A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-Italy
|
Bianchi, Francesca
|
|
2006
|
6 |
1 |
p. 97-102
|
artikel
|
| 4 |
An association between the 4G polymorphism in the PAI-1 promoter and the development of aggressive fibromatosis (desmoid tumor) in familial adenomatous polyposis patients
|
Li, Catherine F.
|
|
2006
|
6 |
1 |
p. 89-95
|
artikel
|
| 5 |
Familial colorectal cancer referral to regional genetics department—a single centre experience
|
Mak, Tony
|
|
2006
|
6 |
1 |
p. 81-87
|
artikel
|
| 6 |
Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data
|
Dijk, D. A. van
|
|
2007
|
6 |
1 |
p. 131-134
|
artikel
|
| 7 |
Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 gene
|
Stewart, W.
|
|
2006
|
6 |
1 |
p. 147-152
|
artikel
|
| 8 |
Heterozygote BRCA1 status and skewed chromosome X inactivation
|
Helbling-Leclerc, Anne
|
|
2006
|
6 |
1 |
p. 153-157
|
artikel
|
| 9 |
Identification of a founder BRCA2 mutation in Sardinian breast cancer families
|
Monne, Maria
|
|
2006
|
6 |
1 |
p. 73-79
|
artikel
|
| 10 |
Improved survival in BRCA2 carriers with ovarian cancer
|
Pal, Tuya
|
|
2006
|
6 |
1 |
p. 113-119
|
artikel
|
| 11 |
Molecular diagnosis of neurofibromatosis type 1: 2 years experience
|
Griffiths, Siân
|
|
2006
|
6 |
1 |
p. 21-34
|
artikel
|
| 12 |
Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from Western Sweden
|
Einbeigi, Zakaria
|
|
2006
|
6 |
1 |
p. 35-41
|
artikel
|
| 13 |
Risks of cancer due to a single BRCA1 mutation in an extended Utah kindred
|
Vogl, Florian D.
|
|
2006
|
6 |
1 |
p. 63-71
|
artikel
|
| 14 |
Study comparing two types of screening provision for people with von Hippel-Lindau disease
|
Fraser, Lindsay
|
|
2006
|
6 |
1 |
p. 103-111
|
artikel
|
| 15 |
The interval between cancer diagnosis among mothers and offspring in a population-based cohort
|
Paltiel, Ora
|
|
2007
|
6 |
1 |
p. 121-129
|
artikel
|
| 16 |
The management of families affected by hereditary non-polyposis colorectal cancer (HNPCC)
|
Geary, Johanne
|
|
2006
|
6 |
1 |
p. 13-19
|
artikel
|
| 17 |
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family
|
Puijenbroek, Marjo van
|
|
2006
|
6 |
1 |
p. 43-51
|
artikel
|
| 18 |
The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome
|
Stuckless, Susan
|
|
2006
|
6 |
1 |
p. 1-12
|
artikel
|
| 19 |
Utility of computed tomographic colonography in surveillance for hereditary nonpolyposis colorectal cancer syndrome
|
Renkonen-Sinisalo, Laura
|
|
2007
|
6 |
1 |
p. 135-140
|
artikel
|
| 20 |
Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies
|
Green, R. C.
|
|
2006
|
6 |
1 |
p. 53-62
|
artikel
|
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