Detection of single clone deletions using array CGH: identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2007）
Key words
array CGH,array comparative genomic hybridization,chromosome 22q,22q11.2 deletion syndrome,genome-wide scan,polymorphism,submicroscopic deletion syndrome
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