| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Chemoprevention in familial adenomatous polyposis: past, present and future
|
Kemp Bohan, Phillip M.
|
|
|
20 |
1 |
p. 23-33
|
artikel
|
| 2 |
Complete response of hereditary leiomyomatosis and renal cell cancer (HLRCC)-associated renal cell carcinoma to nivolumab and ipilimumab combination immunotherapy by: a case report
|
Iribe, Yasuhiro
|
|
|
20 |
1 |
p. 75-80
|
artikel
|
| 3 |
Germline variants discovered in lymphoma patients undergoing tumor profiling: a case series
|
Scott, Anthony J.
|
|
|
20 |
1 |
p. 61-65
|
artikel
|
| 4 |
Improving primary care identification of familial breast cancer risk using proactive invitation and decision support
|
Qureshi, Nadeem
|
|
|
20 |
1 |
p. 13-21
|
artikel
|
| 5 |
Low accuracy of self-reported family history of melanoma in high-risk patients
|
Flint, Nicholas D.
|
|
|
20 |
1 |
p. 41-48
|
artikel
|
| 6 |
Multiple primary cancers (renal papillary, lymphoma and teratoma) and hepatic cysts in association with a pathogenic germline mutation in the MET gene
|
Adlard, Julian
|
|
|
20 |
1 |
p. 81-83
|
artikel
|
| 7 |
New surveillance guidelines for Li-Fraumeni and hereditary TP53 related cancer syndrome: implications for germline TP53 testing in breast cancer
|
Evans, D. Gareth
|
|
|
20 |
1 |
p. 1-7
|
artikel
|
| 8 |
Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD)
|
Seppälä, Toni T.
|
|
|
20 |
1 |
p. 35-39
|
artikel
|
| 9 |
Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019
|
Suerink, M.
|
|
|
20 |
1 |
p. 67-73
|
artikel
|
| 10 |
Small fraction of testicular cancer cases may be causatively related to CHEK2 inactivating germ-line mutations: evidence for somatic loss of the remaining CHEK2 allele in the tumor tissue
|
Ni, Valeriya I.
|
|
|
20 |
1 |
p. 49-53
|
artikel
|
| 11 |
The CAPP II trial of aspirin in Lynch syndrome/HNPCC: is it time for everyone to be treated?
|
Lynch, Patrick M.
|
|
|
20 |
1 |
p. 9-11
|
artikel
|
| 12 |
Two cases of somatic STK11 mosaicism in Danish patients with Peutz–Jeghers syndrome
|
Jelsig, Anne Marie
|
|
|
20 |
1 |
p. 55-59
|
artikel
|
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