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Journal Abstract Search

170 related items for PubMed ID: 22517379

  • 21. 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
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  • 22. 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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  • 23. 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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  • 24. High dimensional endophenotype ranking in the search for major depression risk genes.
    Glahn DC, Curran JE, Winkler AM, Carless MA, Kent JW, Charlesworth JC, Johnson MP, Göring HH, Cole SA, Dyer TD, Moses EK, Olvera RL, Kochunov P, Duggirala R, Fox PT, Almasy L, Blangero J.
    Biol Psychiatry; 2012 Jan 01; 71(1):6-14. PubMed ID: 21982424
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  • 26. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.
    Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF.
    Hum Mol Genet; 2006 Jan 15; 15(2):251-8. PubMed ID: 16330481
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  • 28. Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities.
    Cipriani V, Kalhoro A, Arno G, Silva RS, Pontikos N, Puech V, McClements ME, Hunt DM, van Heyningen V, Michaelides M, Webster AR, Moore AT, Puech B.
    Ophthalmic Genet; 2017 Dec 15; 38(6):511-519. PubMed ID: 28635424
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  • 30. Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.
    Luty AA, Kwok JB, Thompson EM, Blumbergs P, Brooks WS, Loy CT, Dobson-Stone C, Panegyres PK, Hecker J, Nicholson GA, Halliday GM, Schofield PR.
    BMC Neurol; 2008 Aug 29; 8():32. PubMed ID: 18755042
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  • 32. Genome-wide and interaction linkage scan for nonsyndromic cleft lip with or without cleft palate in two multiplex families in Shenyang, China.
    Wang Y, Li X, Zhu WL, Guo JZ, Song XM, Li SQ, Li Y.
    Biomed Environ Sci; 2010 Oct 29; 23(5):363-70. PubMed ID: 21112484
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  • 34. Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD.
    Ross J, Badner J, Garrido H, Sheppard B, Chavira DA, Grados M, Woo JM, Doo P, Umaña P, Fournier E, Murray SS, Mathews CA.
    Hum Genet; 2011 Dec 29; 130(6):795-805. PubMed ID: 21691774
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  • 40. When does speech sound disorder matter for literacy? The role of disordered speech errors, co-occurring language impairment and family risk of dyslexia.
    Hayiou-Thomas ME, Carroll JM, Leavett R, Hulme C, Snowling MJ.
    J Child Psychol Psychiatry; 2017 Feb 29; 58(2):197-205. PubMed ID: 28102620
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