Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma-Reference-Cited by-同舟云学术

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Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma

Published:2019-09 Issue:3 Volume:105 Page:658-668
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Egolf Laura E.,Vaksman Zalman,Lopez Gonzalo,Rokita Jo Lynne,Modi Apexa,Basta Patricia V.,Hakonarson Hakon,Olshan Andrew F.,Diskin Sharon J.

Funder

National Institutes of Health

NIH

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference76 articles.

1. Identification of ALK as a major familial neuroblastoma predisposition gene;Mossé;Nature,2008

2. Germline PHOX2B mutation in hereditary neuroblastoma;Mosse;Am. J. Hum. Genet.,2004

3. Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma;Trochet;Am. J. Hum. Genet.,2004

4. Chromosome 6p22 locus associated with clinically aggressive neuroblastoma;Maris;N. Engl. J. Med.,2008

5. Common variations in BARD1 influence susceptibility to high-risk neuroblastoma;Capasso;Nat. Genet.,2009

Cited by 34 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New Individuals;American Journal of Medical Genetics Part A;2024-09-11

2. Neuroblastoma Predisposition and Surveillance—An Update from the 2023 AACR Childhood Cancer Predisposition Workshop;Clinical Cancer Research;2024-06-11

3. Rare germline structural variants increase risk for pediatric solid tumors;2024-04-29

4. Genetic Predisposition;Pediatric Oncology;2024

5. Health supervision for children and adolescents with 16p11.2 deletion syndrome;Molecular Case Studies;2023-12

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