Genetics of specific language impairment

Prostaglandins Leukotrienes and Essential Fatty Acids

Volumn 63, Issue 1-2, 2000, Pages 101-107

  Nasir, J ^a   Cohen, W ^a   Cowie, H ^a   Maclean, A ^a   Watson, J ^b   Seckl, J ^c   O'Hare, A ^b  

^a WESTERN GENERAL HOSPITAL   (United Kingdom)

^b ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^c UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; GENE; GENE LINKAGE DISEQUILIBRIUM; GENETIC LINKAGE; HUMAN; LANGUAGE DISABILITY; MOLECULAR CLONING; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; QUANTITATIVE TRAIT;

EID: 0033799946     PISSN: 09523278     EISSN: None     Source Type: Journal    
DOI: 10.1054/plef.2000.0199     Document Type: Article

References (52)

1. Genetic basis of specific language impairment: Evidence from a twin study
2. Genetics of spoken language disorders
3. The heritability of language: A review and metaanalysis of twin and adoption studies
4. Is specific language impairment a valid diagnostic category? Genetic and psycholinguistic evidence
5. Language impaired 4-year olds. Distinguished transient form persistent impairment
6. Specific language impairment as a maturation lag: Evidence from longitudinal data on language and motor development
7. Language-impaired preschoolers: A follow up into adolescence
8. The long-term psychological sequelae of specific developmental disorders of speech and language
9. Language comprehension in language impaired children improved with acoustically modified speech
10. Effectiveness of speech intervention for phonological disorders: A randomized controlled trial
11. Different origin of auditory and phonological processing problems in children with language impairment: Evidence from a twin study
12. Deficits in auditory temporal and spectral resolution in language impaired children
13. A grammatical specific language impairment in children: An autosomal dominant inheritance?
14. Binding theory and grammatical specific language impairment in children
15. Evidence for a grammar-specific deficit in children
16. The children's test of nonword repetition: A test of phonological working memory
17. Genetic influence on language delay in two-year old children
18. Localisation of a gene implicated in a severe speech and language disorder
19. Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder
20. Genetic studies of autistic disorder and chromosome 7
21. Genetic dissection of complex traits
22. Polygenic disease: Methods for mapping complex disease traits
23. Invited editorial: Cutting a guardian knot in the linkage analysis of complex human traits
24. A genome wide search for human type 1 diabetes susceptibility genes
25. Identification of deletion mutations and three new genes at the familial polyposis locus
26. The investigation of linkage between a quantitative trait and a marker locus
27. Extreme discordant sib pairs for mapping quantitative trait loci in humans
28. Mapping quantitative trait loci with extreme discordant sib pairs: Sampling considerations
29. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
30. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
31. Nonword repetition as a behavioural marker for inherited language impairment: Evidence from a twin study
32. Genetic isolates: Separate but equal?
33. Prospects for whole-genome linkage disequilibrium mapping of common disease genes
34. MRI findings in the parents and siblings of specifically language-impaired boys
35. Abnormal regional CBF response in left hemisphere of dysphasic children during a language task
36. A new brain region for coordinating speech articulation
37. 1H magnetic resonance spectroscopy
38. Brain regions involved in articulation