19 results on '"Newbury, D. F."'
Search Results
2. Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects
3. Genome-wide screening for DNA variants associated with reading and language traits
4. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
5. Mutation-specific pathophysiological mechanisms in a new SATB1-associated neurodevelopmental disorder
6. Supplement to: A functional genetic link between distinct developmental language disorders
7. A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3
8. Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment
9. Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
10. Copy number variation screen identifies a rare de Novo deletion at chromosome 15q13.1-13.3 in a child with language impairment
11. Genome-wide analysis identifies a role for common copy number variants in specific language impairment
12. Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
13. A genomewide scan identifies two novel loci involved in specific language impairment
14. Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects
15. Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays.
16. Genetic advances in the study of speech and language disorders.
17. Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.
18. Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays.
19. FOXP2 is not a major susceptibility gene for autism or specific language impairment.
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