| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Endoscopic full thickness resection for early colon cancer in Lynch syndrome
|
Langers, Alexandra M. J.
|
|
2019
|
18 |
3 |
p. 349-352
|
artikel
|
| 2 |
Genetic counseling referral for ovarian cancer patients: a call to action
|
Garcia, Christine
|
|
2019
|
18 |
3 |
p. 303-309
|
artikel
|
| 3 |
Hereditary gastric cancer: what’s new? Update 2013–2018
|
van der Post, Rachel S.
|
|
2019
|
18 |
3 |
p. 363-367
|
artikel
|
| 4 |
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting
|
Clarke, Elizabeth V.
|
|
2019
|
18 |
3 |
p. 317-325
|
artikel
|
| 5 |
Implication of DNA repair genes in Lynch-like syndrome
|
Xicola, Rosa M.
|
|
2019
|
18 |
3 |
p. 331-342
|
artikel
|
| 6 |
Moving into the mainstream: healthcare professionals’ views of implementing treatment focussed genetic testing in breast cancer care
|
Hallowell, Nina
|
|
2019
|
18 |
3 |
p. 293-301
|
artikel
|
| 7 |
Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with café-au-lait spots
|
Chiu, Celine
|
|
2019
|
18 |
3 |
p. 353-358
|
artikel
|
| 8 |
Pediatric craniopharyngioma in association with familial adenomatous polyposis
|
Dahl, Nathan A.
|
|
2019
|
18 |
3 |
p. 327-330
|
artikel
|
| 9 |
Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene
|
Beard, Catherine
|
|
2019
|
18 |
3 |
p. 311-315
|
artikel
|
| 10 |
Progress report: familial pancreatic cancer
|
Mintziras, Ioannis
|
|
2019
|
18 |
3 |
p. 359-362
|
artikel
|
| 11 |
Targeted next generation sequencing screening of Lynch syndrome in Tunisian population
|
Ben Sghaier, Rihab
|
|
2019
|
18 |
3 |
p. 343-348
|
artikel
|
| 12 |
The incidence of consecutive manifestations in Von Hippel-Lindau disease
|
Horst-Schrivers, Anouk N. A. van der
|
|
2019
|
18 |
3 |
p. 369-376
|
artikel
|
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