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Cardiac phenotype in the chromosome 22q11.2 microdeletion syndrome

✍ Scribed by Michael Earing; Michael J Ackerman; David J Driscoll

Book ID
114344006
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
71 KB
Volume
15
Category
Article
ISSN
1058-9813

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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