Developmental perspectives on copy number abnormalities of the 22q11.2 region
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01456.x/fullpdf
Reference140 articles.
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2. A common molecular basis for rearrangement disorders on chromosome 22q11;Edelmann;Hum Mol Genet,1999
3. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.;Shaikh;Hum Mol Genet,2000
4. The DNA sequence of human chromosome 22;Dunham;Nature,1999
5. Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions.;Uddin;BMC Med Genet,2006
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