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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
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Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment
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Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment
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Genome-wide screening for DNA variants associated with reading and language traits
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Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
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Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment
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Associations of HLA alleles with specific language impairment
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Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
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Associations of HLA alleles with specific language impairment
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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13 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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BASE
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Show details
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