Airway anomalies in patients with 22q11.2 deletion syndrome: A scoping review
Author:
Funder
Children's Mercy Hospital
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference70 articles.
1. Prevalence of 22q11 microdeletion;Tezenas Du Montcel;J. Med. Genet.,1996
2. A population study of chromosome 22q11 deletions in infancy;Goodship;Arch. Dis. Child.,1998
3. Subglottic web in a mother and son with 22q11.2 deletion;Marble;Am. J. Med. Genet.,1998
4. Practical guidelines for managing patients with 22q11;Bassett;J. Pediatr.,2011
5. Association of airway abnormalities with 22q11.2 deletion syndrome;Sacca;Int. J. Pediatr. Otorhinolaryngol.,2017
Cited by 2 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. Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors;Genes;2024-02-29
2. Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach;International Journal of Molecular Sciences;2023-05-05
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