檢索結果 - Muhammad Imran Shabbir

  • Showing 1 - 2 results of 2
Refine Results
  1. 1
    Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

    Mutations of human TMHS cause recessively inherited non-syndromic hearing loss 由 Muhammad Imran Shabbir, Zubair M. Ahmed, Shahid Y. Khan, Saima Riazuddin, Ali Muhammad Waryah, Shaheen N. Khan, Reyna D Camps, Manju Ghosh, Madulika Kabra, Inna A. Belyantseva, Thomas B. Friedman, Sheikh Riazuddin

    出版 2006
    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:

檢索工具: