Detection of single clone deletions using array CGH: Identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system

Keyphrases

• 22q11.2 Deletion Syndrome 100%
• Array Measurements 33%
• Causal Event 33%
• Chromosome 22 33%
• Copy number Aberrations 33%
• Diagnostic Utility 33%
• Fluorescence in Situ Hybridization Analysis 33%
• Genetic Syndromes 33%
• Genome Scan 66%
• Microdeletion Syndrome 33%
• Single-cell Clone 100%
• Submicroscopic Deletion 100%

Biochemistry, Genetics and Molecular Biology

• Chromosome 22 33%
• Microdeletion Syndrome 33%