Two translocations of chromosome 15q associated with dyslexia.
about
A transcription map of the 6p22.3 reading disability locus identifying candidate genesGenetics of dyslexia: the evolving landscapeThe human lexinome: genes of language and readingA candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brainSupport for EKN1 as the susceptibility locus for dyslexia on 15q21Family-based association study of DYX1C1 variants in autismNo support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexiaAssociation of short-term memory with a variant within DYX1C1 in developmental dyslexiaGenetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficitsA dominant gene for developmental dyslexia on chromosome 3Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.The genetics of reading disabilities: from phenotypes to candidate genesProgress towards a cellular neurobiology of reading disability.The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexiaThe aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and languageRelative burden of large CNVs on a range of neurodevelopmental phenotypes.A theoretical molecular network for dyslexia: integrating available genetic findings.The genetics of developmental dyslexia.Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Developmental dyslexia: genetic dissection of a complex cognitive trait.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.Emerging issues in the genetics of dyslexia: a methodological preview.The first candidate gene for dyslexia: Turning the page of a new chapter of research.Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.Molecular genetics of dyslexia: an overview.Association analysis of dyslexia candidate genes in a Dutch longitudinal sample.An examination of candidate gene SNPs for dyslexia in an Indian sample.CTNND2-a candidate gene for reading problems and mild intellectual disability.Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic lociA Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1
P2860
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P2860
Two translocations of chromosome 15q associated with dyslexia.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
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
2000年论文
@zh
2000年论文
@zh-cn
name
Two translocations of chromosome 15q associated with dyslexia.
@ast
Two translocations of chromosome 15q associated with dyslexia.
@en
type
label
Two translocations of chromosome 15q associated with dyslexia.
@ast
Two translocations of chromosome 15q associated with dyslexia.
@en
prefLabel
Two translocations of chromosome 15q associated with dyslexia.
@ast
Two translocations of chromosome 15q associated with dyslexia.
@en
P2093
P2860
P356
P1476
Two translocations of chromosome 15q associated with dyslexia.
@en
P2093
A E Lehesjoki
A Voutilainen
J Nopola-Hemmi
P2860
P304
P356
10.1136/JMG.37.10.771
P407
P50
P577
2000-10-01T00:00:00Z