| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review
|
Daniell, Julian
|
|
2017
|
17 |
3 |
p. 421-427
|
artikel
|
| 2 |
Association between miR-146a rs2910164 polymorphism and specific cancer susceptibility: an updated meta-analysis
|
Hao, Xia
|
|
2017
|
17 |
3 |
p. 459-468
|
artikel
|
| 3 |
Cancer risk management in Tasmanian women with BRCA1 and BRCA2 mutations
|
Kearton, Stephanie
|
|
2017
|
17 |
3 |
p. 333-344
|
artikel
|
| 4 |
Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries
|
Brédart, Anne
|
|
2017
|
17 |
3 |
p. 469
|
artikel
|
| 5 |
Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics
|
Collet, Gaëlle
|
|
2017
|
17 |
3 |
p. 451-457
|
artikel
|
| 6 |
Ectopic, retroperitoneal adrenocortical carcinoma in the setting of Lynch syndrome
|
Wright, Jesse P.
|
|
2017
|
17 |
3 |
p. 381-385
|
artikel
|
| 7 |
Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer
|
Kallenberg, F. G. J.
|
|
2017
|
17 |
3 |
p. 371-380
|
artikel
|
| 8 |
Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers
|
Goverde, A.
|
|
2017
|
17 |
3 |
p. 361-370
|
artikel
|
| 9 |
Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer
|
Crobach, Stijn
|
|
2017
|
17 |
3 |
p. 415-420
|
artikel
|
| 10 |
Family history influences the tumor characteristics and prognosis of breast cancers developing during postmenopausal hormone therapy
|
Fagerholm, Rainer
|
|
2017
|
17 |
3 |
p. 321-331
|
artikel
|
| 11 |
Genotype phenotype correlation in Asian Indian von Hippel–Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma
|
Lomte, Nilesh
|
|
2017
|
17 |
3 |
p. 441-449
|
artikel
|
| 12 |
Germline mutations in lung cancer and personalized medicine
|
Cetta, Francesco
|
|
2017
|
17 |
3 |
p. 429-430
|
artikel
|
| 13 |
Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma
|
Nistelrooij, A. M. J. van
|
|
2017
|
17 |
3 |
p. 435-440
|
artikel
|
| 14 |
Increased access to TP53 analysis through breast cancer multi-gene panels: clinical considerations
|
Azzollini, Jacopo
|
|
2017
|
17 |
3 |
p. 317-319
|
artikel
|
| 15 |
Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population
|
O’Neill, Suzanne C.
|
|
2017
|
17 |
3 |
p. 351-360
|
artikel
|
| 16 |
Penetrance of a rare familial mutation predisposing to papillary thyroid cancer
|
Saporito, Donika
|
|
2017
|
17 |
3 |
p. 431-434
|
artikel
|
| 17 |
Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge
|
Lynch, Henry T.
|
|
2017
|
17 |
3 |
p. 403-414
|
artikel
|
| 18 |
Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing
|
Soares, Barbara Luísa
|
|
2017
|
17 |
3 |
p. 387-394
|
artikel
|
| 19 |
Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine
|
Myszka, Aleksander
|
|
2017
|
17 |
3 |
p. 345-349
|
artikel
|
| 20 |
Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort
|
González, María Laura
|
|
2017
|
17 |
3 |
p. 395-402
|
artikel
|
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