Works matching IS 00018244 AND DT 2011 AND VI 41 AND IP 1
Results: 17
Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 43, doi. 10.1007/s10519-010-9395-4
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Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 50, doi. 10.1007/s10519-010-9402-9
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Pleiotropic Effects of DCDC2 and DYX1C1 Genes on Language and Mathematics Traits in Nuclear Families of Developmental Dyslexia.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 67, doi. 10.1007/s10519-010-9412-7
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Gene-Environment Interaction in the Etiology of Mathematical Ability Using SNP Sets.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 141, doi. 10.1007/s10519-010-9405-6
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A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 58, doi. 10.1007/s10519-010-9408-3
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Influence of Candidate Genes on Attention Problems in Children: A Longitudinal Study.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 155, doi. 10.1007/s10519-010-9406-5
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- Article
Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 110, doi. 10.1007/s10519-010-9413-6
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Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 90, doi. 10.1007/s10519-010-9424-3
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- Article
An Examination of Candidate Gene SNPs for Dyslexia in an Indian Sample.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 105, doi. 10.1007/s10519-010-9441-2
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SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 134, doi. 10.1007/s10519-010-9431-4
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A Family Based Association Study of DRD4, DAT1, and 5HTT and Continuous Traits of Attention-Deficit Hyperactivity Disorder.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 165, doi. 10.1007/s10519-010-9437-y
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Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 77, doi. 10.1007/s10519-010-9434-1
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Moving Closer to a Public Health Model of Language and Learning Disabilities: The Role of Genetics and the Search for Etiologies.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 1, doi. 10.1007/s10519-010-9439-9
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An Application of the Elastic Net for an Endophenotype Analysis.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 120, doi. 10.1007/s10519-011-9443-8
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In Search of the Perfect Phenotype: An Analysis of Linkage and Association Studies of Reading and Reading-Related Processes.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 6, doi. 10.1007/s10519-011-9444-7
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Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 31, doi. 10.1007/s10519-010-9390-9
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A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 125, doi. 10.1007/s10519-010-9389-2
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