Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: Report of three patients-Reference-Cited by-同舟云学术

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Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: Report of three patients

Published:1997-05-16 Issue:2 Volume:70 Page:130-133
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fokstuen Siv,Bottani Armand,Medeiros Paula F. V.,Antonarakis Stylianos E.,Stoll Claude,Schinzel Albert

Publisher

Wiley

Subject

Genetics(clinical)

Reference20 articles.

1. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

2. Congenital Laryngeal Webs

3. Apparent CHARGE association and chromosome anomaly: Chance or contiguous gene syndrome

4. Congenital Glottic Webs in Children

5. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

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1. Congenital High Airway Obstructive Syndrome (CHAOS) Survival of a Newborn with Laryngeal Atresia;Diagnostics;2023-12-14

2. T-tube implantation combined with cricoid cartilage reconstruction in the treatment of congenital laryngeal webs with subglottic stenosis;European Archives of Oto-Rhino-Laryngology;2023-09-19

3. Evaluation of swallowing in children with higher grades glottic web;European Archives of Oto-Rhino-Laryngology;2023-07-27

4. Airway anomalies in patients with 22q11.2 deletion syndrome: A scoping review;International Journal of Pediatric Otorhinolaryngology;2022-12

5. Otolaryngologic issues in association with 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022

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