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PUBMED FOR HANDHELDS

Journal Abstract Search


172 related items for PubMed ID: 15389766

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  • 2. Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism.
    Avdjieva-Tzavella DM, Todorov TP, Todorova AP, Kirov AV, Hadjidekova SP, Rukova BB, Litvinenko IO, Hristova-Naydenova DN, Tincheva RS, Toncheva DI.
    Genet Couns; 2012; 23(4):505-11. PubMed ID: 23431752
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  • 3. Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?
    Talebizadeh Z, Bittel DC, Veatch OJ, Butler MG, Takahashi TN, Miles JH.
    J Autism Dev Disord; 2004 Dec; 34(6):735-6. PubMed ID: 15679194
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  • 6. Analysis of four neuroligin genes as candidates for autism.
    Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I.
    Eur J Hum Genet; 2005 Dec; 13(12):1285-92. PubMed ID: 16077734
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  • 8. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
    Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T, Paris Autism Research International Sibpair Study.
    Nat Genet; 2003 May; 34(1):27-9. PubMed ID: 12669065
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  • 11. No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level.
    Wermter AK, Kamp-Becker I, Strauch K, Schulte-Körne G, Remschmidt H.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Jun 05; 147B(4):535-7. PubMed ID: 18189281
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  • 13. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.
    Laumonnier F, Bonnet-Brilhault F, Gomot M, Blanc R, David A, Moizard MP, Raynaud M, Ronce N, Lemonnier E, Calvas P, Laudier B, Chelly J, Fryns JP, Ropers HH, Hamel BC, Andres C, Barthélémy C, Moraine C, Briault S.
    Am J Hum Genet; 2004 Mar 05; 74(3):552-7. PubMed ID: 14963808
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  • 14. A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.
    Yu J, He X, Yao D, Li Z, Li H, Zhao Z.
    Behav Brain Funct; 2011 May 14; 7():13. PubMed ID: 21569590
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  • 17. Analysis of the neuroligin 4Y gene in patients with autism.
    Yan J, Feng J, Schroer R, Li W, Skinner C, Schwartz CE, Cook EH, Sommer SS.
    Psychiatr Genet; 2008 Aug 14; 18(4):204-7. PubMed ID: 18628683
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  • 18. Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
    Xu X, Xiong Z, Zhang L, Liu Y, Lu L, Peng Y, Guo H, Zhao J, Xia K, Hu Z.
    Mol Biol Rep; 2014 Jun 14; 41(6):4133-40. PubMed ID: 24570023
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