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PUBMED FOR HANDHELDS

Journal Abstract Search

203 related items for PubMed ID: 27535846

  • 1. Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.
    Truong DT, Shriberg LD, Smith SD, Chapman KL, Scheer-Cohen AR, DeMille MM, Adams AK, Nato AQ, Wijsman EM, Eicher JD, Gruen JR.
    Hum Genet; 2016 Dec; 135(12):1329-1341. PubMed ID: 27535846
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  • 4. The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.
    Strug LJ, Addis L, Chiang T, Baskurt Z, Li W, Clarke T, Hardison H, Kugler SL, Mandelbaum DE, Novotny EJ, Wolf SM, Pal DK.
    PLoS One; 2012 Dec; 7(7):e40696. PubMed ID: 22815793
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  • 5. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits.
    Bates TC, Luciano M, Medland SE, Montgomery GW, Wright MJ, Martin NG.
    Behav Genet; 2011 Jan; 41(1):50-7. PubMed ID: 20949370
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  • 6. Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.
    SLI Consortium (SLIC).
    Am J Hum Genet; 2004 Jun; 74(6):1225-38. PubMed ID: 15133743
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  • 7. Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.
    Peter B, Matsushita M, Raskind WH.
    Psychiatr Genet; 2012 Oct; 22(5):226-34. PubMed ID: 22517379
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  • 8. Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.
    Nöthen MM, Schulte-Körne G, Grimm T, Cichon S, Vogt IR, Müller-Myhsok B, Propping P, Remschmidt H.
    Eur Child Adolesc Psychiatry; 1999 Oct; 8 Suppl 3():56-9. PubMed ID: 10638372
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  • 9. A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.
    Addis L, Friederici AD, Kotz SA, Sabisch B, Barry J, Richter N, Ludwig AA, Rübsamen R, Albert FW, Pääbo S, Newbury DF, Monaco AP.
    Genes Brain Behav; 2010 Aug; 9(6):545-61. PubMed ID: 20345892
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  • 10. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
    Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayán J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, Monaco AP.
    Nat Genet; 2002 Jan; 30(1):86-91. PubMed ID: 11743577
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  • 12. A genomewide scan identifies two novel loci involved in specific language impairment.
    SLI Consortium.
    Am J Hum Genet; 2002 Feb; 70(2):384-98. PubMed ID: 11791209
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  • 18. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.
    de Kovel CG, Hol FA, Heister JG, Willemen JJ, Sandkuijl LA, Franke B, Padberg GW.
    J Med Genet; 2004 Sep; 41(9):652-7. PubMed ID: 15342694
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