Ngā hua rapu - Garner, Shannon

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  1. 1
    De novo missense variant in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy

    De novo missense variant in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy mā Latsko, Maeson S., Koboldt, Daniel C., Franklin, Samuel J., Hickey, Scott E., Williamson, Rachel K., Garner, Shannon, Ostendorf, Adam P., Lee, Kristy, White, Peter, Wilson, Richard K.

    I whakaputaina 2022
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  2. 2
    Saturation mutagenesis defines novel mouse models of severe spine deformity

    Saturation mutagenesis defines novel mouse models of severe spine deformity mā Rios, Jonathan J., Denton, Kristin, Yu, Hao, Manickam, Kandamurugu, Garner, Shannon, Russell, Jamie, Ludwig, Sara, Rosenfeld, Jill A., Liu, Pengfei, Munch, Jake, Sucato, Daniel J., Beutler, Bruce, Wise, Carol A.

    I whakaputaina 2021
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    ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination

    ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination mā Shehata, Laila, Simeonov, Dimitre R., Raams, Anja, Wolfe, Lynne, Vanderver, Adeline, Li, Xueli, Huang, Yan, Garner, Shannon, Boerkoel, Cornelius F., Thurm, Audrey, Herman, Gail E., Tifft, Cynthia J., He, Miao, Jaspers, Nicolaas G.J., Gahl, William A.

    I whakaputaina 2014
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