| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia
|
Cock-Rada, A. M.
|
|
2017
|
17 |
1 |
p. 23-30
|
artikel
|
| 2 |
A single visit multidisciplinary model for managing patients with mutations in moderate and high-risk genes in a community practice setting
|
O’Leary, Michael P.
|
|
2017
|
17 |
1 |
p. 175-178
|
artikel
|
| 3 |
Association of genetic variations in RTN4 3′-UTR with risk for clear cell renal cell carcinoma
|
Pu, Yan
|
|
2017
|
17 |
1 |
p. 129-134
|
artikel
|
| 4 |
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel
|
Abu Freha, Naim
|
|
2017
|
17 |
1 |
p. 79-86
|
artikel
|
| 5 |
Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome
|
Salo-Mullen, Erin E.
|
|
2017
|
17 |
1 |
p. 71-77
|
artikel
|
| 6 |
Co-occurrence of Lynch syndrome and juvenile polyposis syndrome confirmed by multigene panel testing
|
Silva-Smith, Rachel
|
|
2017
|
17 |
1 |
p. 87-90
|
artikel
|
| 7 |
Development of a high risk pancreatic screening clinic using 3.0 T MRI
|
Barnes, Chad A.
|
|
2017
|
17 |
1 |
p. 101-111
|
artikel
|
| 8 |
Early onset renal cell carcinoma in an adolescent girl with germline FLCN exon 5 deletion
|
Schneider, Meike
|
|
2017
|
17 |
1 |
p. 135-139
|
artikel
|
| 9 |
Gestational choriocarcinoma associated with a germline TP53 mutation
|
Brehin, Anne-Claire
|
|
2017
|
17 |
1 |
p. 113-117
|
artikel
|
| 10 |
Heightened perception of breast cancer risk in young women at risk of familial breast cancer
|
Glassey, Rachael
|
|
2017
|
17 |
1 |
p. 15-22
|
artikel
|
| 11 |
How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study
|
Dheensa, Sandi
|
|
2017
|
17 |
1 |
p. 155-166
|
artikel
|
| 12 |
Is there a genetic anticipation in breast and/or ovarian cancer families with the germline c.3481_3491del11 mutation?
|
El Tannouri, R.
|
|
2017
|
17 |
1 |
p. 5-14
|
artikel
|
| 13 |
Next generation sequencing is informing phenotype: a TP53 example
|
O’Shea, R.
|
|
2017
|
17 |
1 |
p. 123-128
|
artikel
|
| 14 |
Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families
|
Dominguez-Valentin, Mev
|
|
2017
|
17 |
1 |
p. 141-153
|
artikel
|
| 15 |
Quality of life following prophylactic gynecological surgery: experiences of female Lynch mutation carriers
|
Etchegary, Holly
|
|
2017
|
17 |
1 |
p. 53-61
|
artikel
|
| 16 |
RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers
|
Fennell, Lochlan J.
|
|
2017
|
17 |
1 |
p. 63-69
|
artikel
|
| 17 |
Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas
|
Clendenning, Mark
|
|
2017
|
17 |
1 |
p. 91-100
|
artikel
|
| 18 |
The association of low penetrance genetic risk modifiers with colorectal cancer in lynch syndrome patients: a systematic review and meta-analysis
|
Donald, Neil
|
|
2017
|
17 |
1 |
p. 43-52
|
artikel
|
| 19 |
The importance of a well-structured pancreatic screening program for familial and hereditary pancreatic cancer
|
Vasen, Hans F. A.
|
|
2017
|
17 |
1 |
p. 1-3
|
artikel
|
| 20 |
The role of screening MRI in the era of next generation sequencing and moderate-risk genetic mutations
|
Macklin, Sarah
|
|
2017
|
17 |
1 |
p. 167-173
|
artikel
|
| 21 |
TP53 germline and somatic mutations in a patient with fibrolamellar hepatocellular carcinoma
|
Andrade, Raissa C.
|
|
2017
|
17 |
1 |
p. 119-122
|
artikel
|
| 22 |
Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries
|
Brédart, Anne
|
|
2017
|
17 |
1 |
p. 31-41
|
artikel
|
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