Hasil Pencarian - Maria H Chahrour

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  1. 1
    Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice

    Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice oleh Laura Dean Heckman, Maria H Chahrour, Huda Y Zoghbi

    Diterbitkan 2014-06-01
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  2. 2
    Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants

    Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants oleh Islam Oguz Tuncay, Nancy L. Parmalee, Raida Khalil, Kiran Kaur, Ashwani Kumar, Mohamed Jimale, Jennifer L. Howe, Kimberly Goodspeed, Patricia Evans, Loai Alzghoul, Chao Xing, Stephen W. Scherer, Maria H. Chahrour

    Diterbitkan 2022-02-01
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  3. 3
    Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.

    Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. oleh Maria H Chahrour, Timothy W Yu, Elaine T Lim, Bulent Ataman, Michael E Coulter, R Sean Hill, Christine R Stevens, Christian R Schubert, ARRA Autism Sequencing Collaboration, Michael E Greenberg, Stacey B Gabriel, Christopher A Walsh

    Diterbitkan 2012-01-01
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  4. 4
    KDM5A mutations identified in autism spectrum disorder using forward genetics

    KDM5A mutations identified in autism spectrum disorder using forward genetics oleh Lauretta El Hayek, Islam Oguz Tuncay, Nadine Nijem, Jamie Russell, Sara Ludwig, Kiran Kaur, Xiaohong Li, Priscilla Anderton, Miao Tang, Amanda Gerard, Anja Heinze, Pia Zacher, Hessa S Alsaif, Aboulfazl Rad, Kazem Hassanpour, Mohammad Reza Abbaszadegan, Camerun Washington, Barbara R DuPont, Raymond J Louie, CAUSES Study, Madeline Couse, Maha Faden, R Curtis Rogers, Rami Abou Jamra, Ellen R Elias, Reza Maroofian, Henry Houlden, Anna Lehman, Bruce Beutler, Maria H Chahrour

    Diterbitkan 2020-12-01
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