Search Results - Maher, Mathew

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  1. 1
    A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families

    A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families by Bronstein, Revital, Capowski, Elizabeth E, Mehrotra, Sudeep, Jansen, Alex D, Navarro-Gomez, Daniel, Maher, Mathew, Place, Emily, Sangermano, Riccardo, Bujakowska, Kinga M, Gamm, David M, Pierce, Eric A

    Published 2020
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  2. 2
    Contribution of non-coding mutations to RPGRIP1-mediated inherited retinal degeneration

    Contribution of non-coding mutations to RPGRIP1-mediated inherited retinal degeneration by Jamshidi, Farzad, Place, Emily M., Mehrotra, Sudeep, Navarro-Gomez, Daniel, Maher, Mathew, Branham, Kari E., Valkanas, Elise, Cherry, Timothy J., Lek, Monkol, MacArthur, Daniel, Pierce, Eric A., Bujakowska, Kinga M.

    Published 2018
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