Search Results - Saba Tasneem

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  1. 1
    SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

    SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis by Saima Anwar, Saima Riazuddin, Zubair M. Ahmed, Saba Tasneem, Ateeq-ul-Jaleel, Shahid Y. Khan, Andrew J. Griffith, Thomas B. Friedman, Sheikh Riazuddin

    Published 2009
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    Artigo
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  2. 2
    Mutations of the<i>RDX</i>gene cause nonsyndromic hearing loss at the<i>DFNB24</i>locus

    Mutations of the<i>RDX</i>gene cause nonsyndromic hearing loss at the<i>DFNB24</i>locus by Shahid Y. Khan, Zubair M. Ahmed, Muhammad Imran Shabbir, Shin‐ichiro Kitajiri, Saeeda Kalsoom, Saba Tasneem, Sara Shayiq, Arabandi Ramesh, Srikumari Srisailpathy, Shaheen N. Khan, Richard J. Smith, Saima Riazuddin, Thomas B. Friedman, Sheikh Riazuddin

    Published 2007
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    Artigo
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  3. 3
    Mutational spectrum of<i>MYO15A</i>: the large N-terminal extension of myosin XVA is required for hearing

    Mutational spectrum of<i>MYO15A</i>: the large N-terminal extension of myosin XVA is required for hearing by N. Nal, Zubair M. Ahmed, Engin Erkal, Özgül M. Alper, Güven Lüleci, Oktay Dinç, Ali Muhammad Waryah, Quratul Ain, Saba Tasneem, Tayyab Husnain, Parna Chattaraj, Saima Riazuddin, Erich T. Boger, Manju Ghosh, Madhulika Kabra, Sheikh Riazuddin, Robert J. Morell, Thomas B. Friedman

    Published 2007
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    Artigo
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