Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference63 articles.
1. Congenital heart defects and 22q11 deletions: which genes count?;Lindsay;Mol. Med. Today,1998
2. The 22q11.2 deletion syndrome;Yamagishi;Keio J. Med.,2002
3. Chromosome microdeletions: dissecting del22q11 syndrome;Lindsay;Nat. Rev. Genet.,2001
4. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis;Shaikh;Hum. Mol. Genet.,2000
5. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region;Lindsay;Am. J. Med. Genet.,1995
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