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Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.
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Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.
Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review. Am J Med Genet A. 2007 Apr 15; 143A(8):791-8.
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PubMed
subject areas
Autistic Disorder
Child
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 7
Forkhead Transcription Factors
Humans
Language Disorders
Male
Microsatellite Repeats
Pedigree
Speech Disorders
authors with profiles
CARLOS BACINO
SAU WAI CHEUNG