Pages that link to "Q35559715"

The following pages link to Two translocations of chromosome 15q associated with dyslexia (Q35559715):

Displaying 40 items.

• A transcription map of the 6p22.3 reading disability locus identifying candidate genes (Q21266625) (← links)
• Genetics of dyslexia: the evolving landscape (Q22306529) (← links)
• The human lexinome: genes of language and reading (Q24653501) (← links)
• A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain (Q24673084) (← links)
• Support for EKN1 as the susceptibility locus for dyslexia on 15q21 (Q28271763) (← links)
• Family-based association study of DYX1C1 variants in autism (Q28286654) (← links)
• No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia (Q28287371) (← links)
• Association of short-term memory with a variant within DYX1C1 in developmental dyslexia (Q28288962) (← links)
• Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits (Q28295739) (← links)
• A dominant gene for developmental dyslexia on chromosome 3 (Q28360966) (← links)
• Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1 (Q28510610) (← links)
• Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments (Q28672682) (← links)
• The genetics of reading disabilities: from phenotypes to candidate genes (Q30459192) (← links)
• Progress towards a cellular neurobiology of reading disability (Q30475697) (← links)
• The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia (Q30482949) (← links)
• The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language (Q30515982) (← links)
• Relative burden of large CNVs on a range of neurodevelopmental phenotypes (Q34079175) (← links)
• A theoretical molecular network for dyslexia: integrating available genetic findings (Q34144455) (← links)
• The genetic basis of dyslexia (Q34212529) (← links)
• The genetics of developmental dyslexia (Q34529947) (← links)
• Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17. (Q34583528) (← links)
• In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes. (Q34666100) (← links)
• Developmental dyslexia: genetic dissection of a complex cognitive trait (Q34932472) (← links)
• Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children (Q35068099) (← links)
• Emerging issues in the genetics of dyslexia: a methodological preview (Q35927117) (← links)
• The first candidate gene for dyslexia: Turning the page of a new chapter of research (Q36160444) (← links)
• Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity (Q36916885) (← links)
• The genetics of reading disability (Q37419588) (← links)
• Genetics of developmental dyslexia (Q37678978) (← links)
• Molecular genetics of dyslexia: an overview (Q38153350) (← links)
• Association analysis of dyslexia candidate genes in a Dutch longitudinal sample (Q39027645) (← links)
• An Examination of Candidate Gene SNPs for Dyslexia in an Indian Sample (Q39797226) (← links)
• CTNND2-a candidate gene for reading problems and mild intellectual disability (Q41729389) (← links)
• Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis. (Q45942481) (← links)
• TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort. (Q52040525) (← links)
• A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia. (Q52058164) (← links)
• Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22. (Q53658316) (← links)
• Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci (Q57323060) (← links)
• A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1 (Q58612547) (← links)
• Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia (Q100559880) (← links)