Clinical variability of the 22q11.2 duplication syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference16 articles.
1. 1.5Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features;Alberti;Clin. Genet.,2007
2. Dissecting contiguous gene defects: TBX1;Baldini;Curr. Opin. Genet. Dev.,2005
3. The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies;de La Rochebrochard;Am. J. Med. Genet. A,2006
4. A common molecular basis for rearrangement disorders on chromosome 22q11;Edelmann;Hum. Mol. Genet.,1999
5. DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation;Engels;Neurology,2007
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