Nasal dimple as part of the 22q11.2 deletion syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference11 articles.
1. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
2. Frontonasal dysplasia associated with tetralogy of Fallot.
3. Family studies in chromosome 22q11 deletion: further demonstration of phenotypic heterogeneity
4. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
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1. Craniofacial abnormalities in association with 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022
2. 22q11.2 deletion syndrome: Setting the stage;The Chromosome 22q11.2 Deletion Syndrome;2022
3. Nasal Dimple as a Rare Phenotype of Digeroge Syndrome: Revisited;The Indian Journal of Pediatrics;2017-09-19
4. Genetics of Common Congenital Syndromes of the Head and Neck;Congenital Malformations of the Head and Neck;2013-11-09
5. Prenatal diagnosis of a nasal cyst in association with deletion 22q11 syndrome: a report of two cases;Prenatal Diagnosis;2011-06-28
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