Audiological Findings in Patients with Microdeletion 22Qll (Di George/Velocardiofacial Syndrome)
Author:
Publisher
Informa UK Limited
Subject
Otorhinolaryngology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03005369909090116
Reference17 articles.
1. Aural Abnormalities in Partial DiGeorge Syndrome
2. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations
3. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
4. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
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2. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03
3. Primary pediatric care for children and youth with 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022
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5. Case Report: Challenging Otologic Surgery in Patients With 22q11.2 Deletion Syndrome;Frontiers in Surgery;2020-08-18
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