Comparison of clinical selection-based genetic testing with phenotype-agnostic extensive germline sequencing to diagnose genetic predisposition in children with cancer: a prospective diagnostic study-Reference-Cited by-同舟云学术

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Comparison of clinical selection-based genetic testing with phenotype-agnostic extensive germline sequencing to diagnose genetic predisposition in children with cancer: a prospective diagnostic study

Published:2024-08 Issue: Volume: Page:
ISSN:2352-4642
Container-title:The Lancet Child & Adolescent Health
language:en
Short-container-title:The Lancet Child & Adolescent Health

Author:

Bakhuizen Jette J,van Dijk Freerk,Koudijs Marco J,Bladergroen Reno S,Bon Sebastian B B,Hopman Saskia M J,Kester Lennart A,Kranendonk Mariëtte E G,Loeffen Jan L C,Smetsers Stephanie E,Sonneveld Edwin,Tachdjian Melissa,de Vos-Kerkhof Evelien,Goudie Catherine,Merks Johannes H M,Kuiper Roland P,Jongmans Marjolijn C J

Funder

Stichting Kinderen Kankervrij

Publisher

Elsevier BV

Reference29 articles.

1. Predisposition to cancer in children and adolescents;Kratz;Lancet Child Adolesc Health,2021

2. Recognition of genetic predisposition in pediatric cancer patients: an easy-to-use selection tool;Jongmans;Eur J Med Genet,2016

3. Childhood cancer predisposition syndromes—a concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology;Ripperger;Am J Med Genet A,2017

4. Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study;Postema;Fam Cancer,2021

5. The McGill Interactive Pediatric OncoGenetic Guidelines: an approach to identifying pediatric oncology patients most likely to benefit from a genetic evaluation;Goudie;Pediatr Blood Cancer,2017

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