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                             14 gevonden resultaten
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 Fr├╝hwald, 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
                             14 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland