| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer
|
Ripperger, Tim
|
|
|
20 |
4 |
p. 289-291
|
artikel
|
| 2 |
Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study
|
Postema, Floor A. M.
|
|
|
20 |
4 |
p. 263-271
|
artikel
|
| 3 |
Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma
|
van Engelen, N.
|
|
|
20 |
4 |
p. 349-354
|
artikel
|
| 4 |
Correction to: Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer
|
Ripperger, Tim
|
|
|
20 |
4 |
p. 293
|
artikel
|
| 5 |
Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG)
|
Guerrini-Rousseau, L.
|
|
|
20 |
4 |
p. 317-325
|
artikel
|
| 6 |
Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group
|
Frühwald, M. C.
|
|
|
20 |
4 |
p. 305-316
|
artikel
|
| 7 |
Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire
|
Schwermer, Miriam
|
|
|
20 |
4 |
p. 257-262
|
artikel
|
| 8 |
Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group
|
Hettmer, Simone
|
|
|
20 |
4 |
p. 327-336
|
artikel
|
| 9 |
Ovarian carcinoma in children with constitutional mutation of SMARCA4: single-family report and literature review
|
Pastorczak, Agata
|
|
|
20 |
4 |
p. 355-362
|
artikel
|
| 10 |
Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features
|
Nguyen, Thi Minh Kha
|
|
|
20 |
4 |
p. 273-277
|
artikel
|
| 11 |
Review of guidelines for the identification and clinical care of patients with genetic predisposition for hematological malignancies
|
Schlegelberger, Brigitte
|
|
|
20 |
4 |
p. 295-303
|
artikel
|
| 12 |
Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel
|
Byrjalsen, Anna
|
|
|
20 |
4 |
p. 279-287
|
artikel
|
| 13 |
Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group
|
Bakhuizen, Jette J.
|
|
|
20 |
4 |
p. 337-348
|
artikel
|
| 14 |
The paradigm of hematological malignant versus non-malignant manifestations, driven by primary immunodeficiencies: a complex interplay
|
Kelaidi, C.
|
|
|
20 |
4 |
p. 363-380
|
artikel
|
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