Torthaí cuardaigh - 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 de réir 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

    Foilsithe / Cruthaithe 2019
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    Errata/Corrigenda
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  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 de réir 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

    Foilsithe / Cruthaithe 2019
    Faigh an téacs iomlán
    Artigo
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