Erratum: Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization (Genetics in Medicine (2012) 14:11 (928-936) DOI: 10.1038/gim.2012.72);Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization

Genetics in Medicine

Volumn 14, Issue 11, 2012, Pages 928-936

  Laffin, Jennifer J S ^a,b   Raca, Gordana ^c   Jackson, Craig A ^a,b   Strand, Edythe A ^d   Jakielski, Kathy J ^e   Shriberg, Lawrence D ^a,f  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b WISCONSIN STATE LABORATORY OF HYGIENE   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

^d MAYO CLINIC   (United States)

^e AUGUSTANA COLLEGE   (United States)

^f UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

16p11.2; apraxia; dyspraxia; FOXP2; speech disorder

Indexed keywords

TRANSCRIPTION FACTOR FOXP2;

ADOLESCENT; APRAXIA; ARTICLE; CHILD; CHILDHOOD APRAXIA OF SPEECH; CHROMOSOME 13; CHROMOSOME 14; CHROMOSOME 2; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DISEASE SEVERITY; FEMALE; GENE MUTATION; HUMAN; LANGUAGE DISABILITY; PRESCHOOL CHILD; RARE DISEASE; SCHOOL CHILD; SPEECH ANALYSIS; SPEECH DISORDER;

EID: 84869074313     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1038/gim.2013.85     Document Type: Erratum

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