The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
about
The genetics of autistic disorders and its clinical relevance: a review of the literatureGenetics of austim: complex aetiology for a heterogeneous disorderChromosome 7q: where autism meets language disorder?FOXP2 is not a major susceptibility gene for autism or specific language impairmentFOXP2Human chromosome 7: DNA sequence and biologyA locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.Genetic advances in the study of speech and language disordersA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersThe human lexinome: genes of language and readingAbsence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaNeurogenomics of speech and language disorders: the road aheadRecent and ongoing selection in the human genomeMultiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersFamily-based association study of DYX1C1 variants in autismFOXP2 and the neuroanatomy of speech and languageDisruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndromeChromosomal Rearrangements as Barriers to Genetic Homogenization between Archaic and Modern HumansRecent advances in the genetics of language impairmentCentral timing deficits in subtypes of primary speech disorders.Linking neurogenetics and individual differences in language learning: the dopamine hypothesis.Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridizationAssociation of specific language impairment (SLI) to the region of 7q31.Evaluation of FOXP2 as an autism susceptibility gene.A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9pRisk factors for speech delay of unknown origin in 3-year-old children.Genetic insights into the functional elements of language.Developmental dyslexia: genetic dissection of a complex cognitive trait.Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.Genetic studies of stuttering in a founder populationThe eloquent ape: genes, brains and the evolution of language.Maternal infection leads to abnormal gene regulation and brain atrophy in mouse offspring: implications for genesis of neurodevelopmental disordersA genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13Salivary FOXP2 expression and oral feeding success in premature infantsLanguage growth and genetics of specific language impairment.Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.A genomewide scan identifies two novel loci involved in specific language impairmentLanguage features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2
P2860
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P2860
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
description
2000 nî lūn-bûn
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2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
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2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
The SPCH1 region on human 7q31 ...... h speech and language disorder
@ast
The SPCH1 region on human 7q31 ...... h speech and language disorder
@en
The SPCH1 region on human 7q31 ...... h speech and language disorder
@nl
type
label
The SPCH1 region on human 7q31 ...... h speech and language disorder
@ast
The SPCH1 region on human 7q31 ...... h speech and language disorder
@en
The SPCH1 region on human 7q31 ...... h speech and language disorder
@nl
prefLabel
The SPCH1 region on human 7q31 ...... h speech and language disorder
@ast
The SPCH1 region on human 7q31 ...... h speech and language disorder
@en
The SPCH1 region on human 7q31 ...... h speech and language disorder
@nl
P2093
P2860
P50
P356
P1476
The SPCH1 region on human 7q31 ...... h speech and language disorder
@en
P2093
D C Jamison
S Jeremiah
P2860
P304
P356
10.1086/303011
P407
P577
2000-07-05T00:00:00Z