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4. A forkhead-domain gene is mutated in a severe speech and language disorder. Lai CS; Fisher SE; Hurst JA; Vargha-Khadem F; Monaco AP Nature; 2001 Oct; 413(6855):519-23. PubMed ID: 11586359 [TBL] [Abstract][Full Text] [Related]
6. Localisation of a gene implicated in a severe speech and language disorder. Fisher SE; Vargha-Khadem F; Watkins KE; Monaco AP; Pembrey ME Nat Genet; 1998 Feb; 18(2):168-70. PubMed ID: 9462748 [TBL] [Abstract][Full Text] [Related]
7. The search for autism disease genes. Wassink TH; Brzustowicz LM; Bartlett CW; Szatmari P Ment Retard Dev Disabil Res Rev; 2004; 10(4):272-83. PubMed ID: 15666342 [TBL] [Abstract][Full Text] [Related]
8. Examination of candidate genes in language disorder: a model of genetic association for treatment studies. Haines J; Camarata S Ment Retard Dev Disabil Res Rev; 2004; 10(3):208-17. PubMed ID: 15611983 [TBL] [Abstract][Full Text] [Related]
9. Expressive and receptive vocabulary in children with Williams and Down syndromes. Ypsilanti A; Grouios G; Alevriadou A; Tsapkini K J Intellect Disabil Res; 2005 May; 49(Pt 5):353-64. PubMed ID: 15817052 [TBL] [Abstract][Full Text] [Related]
11. Prevalence of unsuspected language disorders in a child psychiatric population. Cohen NJ; Davine M; Meloche-Kelly M J Am Acad Child Adolesc Psychiatry; 1989 Jan; 28(1):107-11. PubMed ID: 2914822 [TBL] [Abstract][Full Text] [Related]
12. Effects of sampling context on the expressive language of children and adolescents with mental retardation. Abbeduto L; Benson G; Short K; Dolish J Ment Retard; 1995 Oct; 33(5):279-88. PubMed ID: 7476250 [TBL] [Abstract][Full Text] [Related]
13. Low expressive vocabulary: higher heritability as a function of more severe cases. DeThorne LS; Petrill SA; Hayiou-Thomas ME; Plomin R J Speech Lang Hear Res; 2005 Aug; 48(4):792-804. PubMed ID: 16378474 [TBL] [Abstract][Full Text] [Related]
14. Talk of genetics and vice versa. Pinker S Nature; 2001 Oct; 413(6855):465-6. PubMed ID: 11586336 [No Abstract] [Full Text] [Related]
15. Chromosome 7q: where autism meets language disorder? Folstein SE; Mankoski RE Am J Hum Genet; 2000 Aug; 67(2):278-81. PubMed ID: 10889044 [No Abstract] [Full Text] [Related]
16. Stephanie's story: caring for a child with terminal 22q deletion syndrome. Axel SM; Wermuth KG Pediatrics; 2005 Feb; 115(2):512. PubMed ID: 15687465 [No Abstract] [Full Text] [Related]
17. 49,XXXXY syndrome: behavioural and developmental profiles. Lomelino CA; Reiss AL J Med Genet; 1991 Sep; 28(9):609-12. PubMed ID: 1956059 [TBL] [Abstract][Full Text] [Related]
18. Revaluation twenty-three years later of a supernumerary derivative chromosome 9. Yardin C; Esclaire F; Terro F; Barthe D; Gilbert B Am J Med Genet; 2002 Aug; 111(2):213-4. PubMed ID: 12210354 [No Abstract] [Full Text] [Related]
19. Incorporating language phenotypes strengthens evidence of linkage to autism. Collaborative Linkage Study of Autism Am J Med Genet; 2001 Dec; 105(8):539-47. PubMed ID: 11811141 [TBL] [Abstract][Full Text] [Related]
20. Genes, language development, and language disorders. Smith SD Ment Retard Dev Disabil Res Rev; 2007; 13(1):96-105. PubMed ID: 17326114 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]