3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination

Published 2013 View Full Article

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Title
3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination
Authors
Keywords
-
Journal
GENE
Volume 516, Issue 1, Pages 107-113
Publisher
Elsevier BV
Online
2013-01-01
DOI
10.1016/j.gene.2012.12.073

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