Velopharyngeal insufficiency: high detection rate of genetic abnormalities if associated with additional features
Author:
Publisher
BMJ
Subject
Pediatrics, Perinatology and Child Health
Reference17 articles.
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2. Noncleft velopharyngeal insufficiency: etiology and need for surgical treatment;Goudy;Int J Otolaryngol,2012
3. Otolaryngologic manifestations of the 22q11.2 deletion syndrome;Dyce;Arch Otolaryngol Head Neck Surg,2002
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5. Velopharyngeal incompetence: a guide for clinical evaluation;Johns;Plast Reconstr Surg,2003
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1. Quality of Life in Patients With Velopharyngeal Insufficiency in West China;The Cleft Palate-Craniofacial Journal;2021-08-30
2. KBG syndrome: Common and uncommon clinical features based on 31 new patients;American Journal of Medical Genetics Part A;2020-03-03
3. Musculo-mucous web velum and velopharyngeal dysfunction associated with 8q22.1–22.2 microduplication;International Journal of Pediatric Otorhinolaryngology;2018-01
4. Insuffisance vélaire;ORL Chez L'enfant;2017
5. Management of developmental speech and language disorders: Part 1;Archives of Disease in Childhood;2015-07-24
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