檢索結果 - Saba Tasneem

  • Showing 1 - 3 results of 3
Refine Results
  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 由 Saima Anwar, Saima Riazuddin, Zubair M. Ahmed, Saba Tasneem, Ateeq-ul-Jaleel, Shahid Y. Khan, Andrew J. Griffith, Thomas B. Friedman, Sheikh Riazuddin

    出版 2009
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 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

    出版 2007
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 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

    出版 2007
    獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: