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Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype

✍ Scribed by N Hoppman-Chaney; K Wain; PR Seger; DW Superneau; JC Hodge

Book ID
119839667
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
876 KB
Volume
83
Category
Article
ISSN
0009-9163

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## Abstract A broad spectrum of neurodevelopmental and psychiatric disorders with variable expressivity has been reported to be associated with 15q13.3 heterozygous microdeletions. Using oligonucleotide‐based array‐CGH analysis, we identified a small homozygous 15q13.3 deletion in a 6‐year‐old girl