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Cayler cardiofacial syndrome and del22qll: Part of the CATCH22 phenotype

✍ Scribed by Giannotti, Aldo ;Digilio, Maria Cristina ;Marino, Bruno ;Mingarelli, Rita ;Dallapiccola, Bruno


Book ID
101448041
Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
177 KB
Volume
53
Category
Article
ISSN
0148-7299

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## Communicated by Riccardo Fodde The 22q11.2 microdeletion syndrome is the most frequent microdeletion syndrome in humans, yet its genetic basis is complex and is still not fully understood. Most patients harbor a 3-Mb deletion (typically deleted region [TDR]), but occasionally patients with atypi