Velopharyngeal incompetence and chromosome 22q11 deletion
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Minimum prevalence of chromosome 22q11 deletions;Wilson;Am J Hum Genet,1994
2. Fetal echocardiography as a predictor of chromosomal abnormality;Raymond;Lancet,1997
3. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome;Driscoll;Am J Med Genet,1992
4. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study;Ryan;J Med Genet,1997
5. Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency;Zori;Am J Med Genet,1998
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1. Multiple Intestinal Anomalies in a Newborn with 22q11.2 Microdeletion Syndrome: A Case Report and Literature Review;Journal of Pediatric Genetics;2022-08-02
2. 22q11.2 deletion syndrome: Setting the stage;The Chromosome 22q11.2 Deletion Syndrome;2022
3. Velopharyngeal Dysfunction;Cummings Pediatric Otolaryngology;2021
4. Identification of relevant International Classification of Functioning Disability and Health (ICF) categories in patients with 22q11.2 Deletion Syndrome: a Delphi exercise;CoDAS;2020
5. Non-cleft Velopharyngeal Insufficiency;Multidisciplinary Management of Pediatric Voice and Swallowing Disorders;2019-11-17
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