Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33749/fullpdf
Reference40 articles.
1. Genome-wide analyses of human perisylvian cerebral cortical patterning;Abrahams;Proc Natl Acad Sci USA,2007
2. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene;Alarcon;Am J Hum Genet,2008
3. Genetic aspects of early childhood stuttering;Ambrose;J Speech Hear Res,1993
4. The nature of stuttering;Andrews;Med J Aust,1964
5. Genetic factors in stuttering confirmed;Andrews;Arch Gen Psychiatry,1991
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