Search Results - Chonchaiya, W

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  1. 1
    Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome

    Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome by Chonchaiya, W, Nguyen, DV, Au, J, Campos, L, Berry-Kravis, EM, Lohse, K, Mu, Y, Utari, A, Hervey, C, Wang, L, Sorensen, P, Cook, K, Gane, L, Tassone, F, Hagerman, RJ

    Published in Clinical genetics
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  2. 2
    Development of Computerized Tool for Screening Thai Children at Risk for Learning Disabilities

    Development of Computerized Tool for Screening Thai Children at Risk for Learning Disabilities by Munthuli, A, Anansiripinyo, T, Klangpornkun, N, Onsuwan, C, Chonchaiya, W, Trairatvorakul, P, Jitrotjanarak, J, Voracharusrungsi, P, Atichatthanin, N, Tantibundhit, C

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  3. 3
    Integrated genome-wide Alu methylation and transcriptome profiling analyses reveal novel epigenetic regulatory networks associated with autism spectrum disorder

    Integrated genome-wide Alu methylation and transcriptome profiling analyses reveal novel epigenetic regulatory networks associated with autism spectrum disorder by Saeliw, Thanit, Tangsuwansri, Chayanin, Thongkorn, Surangrat, Chonchaiya, Weerasak, Suphapeetiporn, Kanya, Mutirangura, Apiwat, Tencomnao, Tewin, Hu, Valerie W, Sarachana, Tewarit

    Published in Molecular autism
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  4. 4
    Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder

    Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder by Chonchaiya, Weerasak, Au, Jacky, Schneider, Andrea, Hessl, David, Harris, Susan W., Laird, Meredith, Mu, Yi, Tassone, Flora, Nguyen, Danh V., Hagerman, Randi J.

    Published in Human genetics
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