| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency
|
Wimmer, Katharina
|
|
2016
|
16 |
1 |
p. 67-71
|
artikel
|
| 2 |
Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer
|
Elsaid, Afaf
|
|
2016
|
16 |
1 |
p. 83-90
|
artikel
|
| 3 |
BRCA testing within the Department of Veterans Affairs: concordance with clinical practice guidelines
|
Chun, Danielle S.
|
|
2016
|
16 |
1 |
p. 41-49
|
artikel
|
| 4 |
Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers
|
Eijkelenkamp, Karin
|
|
2016
|
16 |
1 |
p. 123-130
|
artikel
|
| 5 |
Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort
|
Jarhelle, Elisabeth
|
|
2016
|
16 |
1 |
p. 1-16
|
artikel
|
| 6 |
Community attitudes towards a Jewish community BRCA1/2 testing program
|
Cousens, Nicole
|
|
2016
|
16 |
1 |
p. 17-28
|
artikel
|
| 7 |
Dilemmas in the management of screen-detected lesions in patients at high risk for pancreatic cancer
|
Ibrahim, Isaura S.
|
|
2016
|
16 |
1 |
p. 111-115
|
artikel
|
| 8 |
Do women change their breast cancer mammogram screening behaviour after BRCA1/2 testing?
|
Larouche, Geneviève
|
|
2016
|
16 |
1 |
p. 35-40
|
artikel
|
| 9 |
Exploring clinicians’ attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancer
|
Chen, Yanni
|
|
2016
|
16 |
1 |
p. 99-109
|
artikel
|
| 10 |
Factors associated with cancer worries in individuals participating in annual pancreatic cancer surveillance
|
Konings, Ingrid C.A.W.
|
|
2016
|
16 |
1 |
p. 143-151
|
artikel
|
| 11 |
First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome
|
Ziada-Bouchaar, H.
|
|
2016
|
16 |
1 |
p. 57-66
|
artikel
|
| 12 |
Frequency of germline PALB2 mutations among women with epithelial ovarian cancer
|
Kotsopoulos, Joanne
|
|
2016
|
16 |
1 |
p. 29-34
|
artikel
|
| 13 |
Genetically diagnosed Birt–Hogg–Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report
|
Whitworth, James
|
|
2016
|
16 |
1 |
p. 139-142
|
artikel
|
| 14 |
Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling
|
Benusiglio, Patrick R.
|
|
2016
|
16 |
1 |
p. 51-56
|
artikel
|
| 15 |
Hereditary leiomyomatosis and renal cell cancer syndrome: identification and clinical characterization of a novel mutation in the FH gene in a Colombian family
|
Arenas Valencia, Carolina
|
|
2016
|
16 |
1 |
p. 117-122
|
artikel
|
| 16 |
Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program
|
Hermel, David J.
|
|
2016
|
16 |
1 |
p. 159-166
|
artikel
|
| 17 |
Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases
|
Hamadou, Walid Sabri
|
|
2016
|
16 |
1 |
p. 153-157
|
artikel
|
| 18 |
Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene
|
Kato, Chise
|
|
2016
|
16 |
1 |
p. 131-138
|
artikel
|
| 19 |
Pancreas-sparing total duodenectomy for Spigelman stage IV duodenal polyposis associated with familial adenomatous polyposis: experience of 10 cases at a single institution
|
Watanabe, Yuichiro
|
|
2016
|
16 |
1 |
p. 91-98
|
artikel
|
| 20 |
Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression
|
Cabreira, Verónica
|
|
2016
|
16 |
1 |
p. 73-81
|
artikel
|
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