A novel microdeletion, del(2)(q22.3q23.3) in a mentally retarded patient, detected by array-based comparative genomic hybridization
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference18 articles.
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3. Interstitial deletion of the long arm of chromosome 2: a clinically recognizable microdeletion syndrome?;Maas;Clin Dysmorphol,2000
4. ‘Mowat-Wilson’ syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies - mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene;Zweier;Am J Med Genet,2002
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