Surgical insights and management in patients with the 22q11.2 deletion syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00383-022-05123-0.pdf
Reference32 articles.
1. Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B (1999) Microdeletion 22q11 and oesophageal atresia. J Med Genet 36(2):137–139
2. McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JAS et al (2015) 22q11.2 deletion syndrome. Nat Rev Dis Primers 1:15071
3. Zemble R, Luning Prak E, McDonald K, McDonald-McGinn D, Zackai E, Sullivan K (2010) Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). Clin Immunol 136(3):409–418
4. McDonald-McGinn DM, LaRossa D, Goldmuntz E, Sullivan K, Eicher P, Gerdes M et al (1997) The 22q11. 2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients. Genet Test 1(2):99–108
5. Eicher PS, McDonald-McGinn DM, Fox CA, Driscoll DA, Emanuel BS, Zackai EH (2000) Dysphagia in children with a 22q11 2 deletion: unusual pattern found on modified barium swallow. J Pediatrics 137(2):158–164
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