Pages that link to "Q31988981"

The following pages link to Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set. (Q31988981):

Displaying 37 items.

• Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation (Q24539066) (← links)
• DCDC2 genetic variants and susceptibility to developmental dyslexia (Q24631569) (← links)
• A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain (Q24673084) (← links)
• A new gene (DYX3) for dyslexia is located on chromosome 2 (Q24681637) (← links)
• Genome scan for linkage to Gilles de la Tourette syndrome (Q28139418) (← links)
• The genetics of reading disabilities: from phenotypes to candidate genes (Q30459192) (← links)
• Genetic susceptibility to neurodevelopmental disorders (Q33586418) (← links)
• Reading and spelling disorders: clinical features and causes (Q33819264) (← links)
• Linkage analysis of Tourette syndrome in a large Utah pedigree (Q34073116) (← links)
• Segregation analysis of phenotypic components of learning disabilities. I. Nonword memory and digit span (Q34142634) (← links)
• Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: confirmation of qualitative analyses (Q34145205) (← links)
• Aryl hydrocarbon receptor nuclear translocator 2 (ARNT2): structure, gene mapping, polymorphisms, and candidate evaluation for human orofacial clefts (Q34147565) (← links)
• Specific reading disability: a multiplanar view (Q34176618) (← links)
• The genetic basis of dyslexia (Q34212529) (← links)
• Tics and its disorders (Q34353578) (← links)
• A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia (Q34388570) (← 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)
• Evidence for linkage and association with reading disability on 6p21.3-22. (Q35764638) (← links)
• Emerging issues in the genetics of dyslexia: a methodological preview (Q35927117) (← links)
• Association of the ROBO1 gene with reading disabilities in a family-based analysis. (Q37059739) (← links)
• Genetics of developmental dyslexia (Q37678978) (← links)
• A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1. (Q37738889) (← links)
• Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects (Q42613559) (← links)
• The effect of consanguineous marriage on reading disability in the Arab community (Q43656564) (← links)
• Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36. (Q48276055) (← links)
• Familial dyslexia in a large Swedish family: a whole genome linkage scan (Q48531897) (← links)
• Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia (Q48654809) (← links)
• Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design (Q52050854) (← links)
• Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses (Q52089574) (← links)
• Etiology of neuroanatomical correlates of reading disability (Q52163540) (← links)
• Neurodevelopmental dysfunction and specific learning disabilities in school-aged twins (Q52166443) (← 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 complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. The Tourette Syndrome Association International Consortium for Genetics (Q73082928) (← links)