Canlyniadau Chwilio - Senthuri Viththiyapaskaran

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  1. 1
    Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease

    Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease gan Hernán Gonorazky, Sergey Naumenko, Arun Ramani, Viswateja Nelakuditi, Pouria Mashouri, Peiqui Wang, Dennis Kao, Krish Ohri, Senthuri Viththiyapaskaran, Mark A. Tarnopolsky, Katherine D. Mathews, Steven A. Moore, Andres Nascimiento Osorio, David Villanova, Dwi U. Kemaladewi, Ronald D. Cohn, Michael Brudno, James J. Dowling

    Cyhoeddwyd 2019
    Cael y testun llawn Cael y testun llawn
    Errata/Corrigenda
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  2. 2
    Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease

    Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease gan Hernán Gonorazky, Sergey Naumenko, Arun Ramani, Viswateja Nelakuditi, Pouria Mashouri, Peiqui Wang, Dennis Kao, Krish Ohri, Senthuri Viththiyapaskaran, Mark A. Tarnopolsky, Katherine D. Mathews, Steven A. Moore, Andres Nascimiento Osorio, David Villanova, Dwi U. Kemaladewi, Ronald D. Cohn, Michael Brudno, James J. Dowling

    Cyhoeddwyd 2019
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:

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