| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A coordinated multidisciplinary model of care is needed for child and family centered care in pediatric genetic cancer risk services: a scoping review
|
Grant, Andrew M.
|
|
|
24 |
3 |
|
artikel
|
| 2 |
Completeness of colorectal cancer registration in the Danish hereditary non-polyposis colorectal cancer (HNPCC) register
|
Lindberg, Lars Joachim
|
|
|
24 |
3 |
|
artikel
|
| 3 |
Copy number and structural variant analyses of VHL gene using droplet digital PCR and targeted adaptive sampling long-read sequencing
|
Kato, Shota
|
|
|
24 |
3 |
|
artikel
|
| 4 |
Experiences with risk-reducing mastectomy in Norwegian BRCA1/2 carriers without prior breast cancer
|
Hyldebrandt, Hanne Kjensli
|
|
|
24 |
3 |
|
artikel
|
| 5 |
Gastric-type endocervical adenocarcinoma in situ as the presenting feature in a mosaic STK11 pathogenic variant carrier with a Peutz-Jeghers syndrome child
|
Jiang, Anqi
|
|
|
24 |
3 |
|
artikel
|
| 6 |
MLH1 c.27G>A (p.Arg9=) is a synonymous likely/pathogenic variant underlying variably mosaic constitutional MLH1 methylation in Lynch syndrome
|
Alvarez, Rocio
|
|
|
24 |
3 |
|
artikel
|
| 7 |
Parental perspectives on the use of tumor molecular profiling and germline genetic testing during their children's cancer treatment
|
Sleiman, Marcelo M.
|
|
|
24 |
3 |
|
artikel
|
| 8 |
Rate of germline pathogenic sequence variants in cancer susceptibility genes in an Israeli pediatric and adolescent cancer cohort: a single institute experience
|
Nahom, Dana
|
|
|
24 |
3 |
|
artikel
|
| 9 |
SMARCB1-related schwannomatosis and other SMARCB1-associated phenotypes: clinical spectrum and molecular pathogenesis
|
Kehrer-Sawatzki, Hildegard
|
|
|
24 |
3 |
|
artikel
|
| 10 |
Updates and controversies for desmoids in familial adenomatous polyposis
|
Aoun, Rami James N.
|
|
|
24 |
3 |
|
artikel
|
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