Is Isolated Palatal Anomaly an Indication to Screen for 22q11 Region Deletion?
Author:
Publisher
SAGE Publications
Subject
Otorhinolaryngology,Oral Surgery
Reference36 articles.
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1. The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review;Journal of Pediatric Genetics;2019-10-23
2. 22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate;The Cleft Palate-Craniofacial Journal;2018-04-13
3. Clinical Features in Patients with 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities;The Cleft Palate-Craniofacial Journal;2015-07
4. Classification, Epidemiology, and Genetics of Orofacial Clefts;Clinics in Plastic Surgery;2014-04
5. Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature;European Journal of Pediatrics;2013-02-26
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