Hasil Pencarian - Riazuddin Saima

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  1. 1
    Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population

    Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population oleh Jaworek Thomas J, Kausar Tasleem, Bell Shannon M, Tariq Nabeela, Maqsood Muhammad, Sohail Asma, Ali Muhmmmad, Iqbal Furhan, Rasool Shafqat, Riazuddin Saima, Shaikh Rehan S, Ahmed Zubair M

    Diterbitkan 2012-06-01
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  2. 2
    Variable expressivity of <it>FGF3 </it>mutations associated with deafness and LAMM syndrome

    Variable expressivity of <it>FGF3 </it>mutations associated with deafness and LAMM syndrome oleh Griffith Andrew J, Butman John A, Riazuddin Sheikh, Shaukat Uzma, Nasir Idrees, Khan Shaheen N, Hegde Rashmi S, Ahmed Zubair M, Riazuddin Saima, Friedman Thomas B, Choi Byung

    Diterbitkan 2011-02-01
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  3. 3
    Characterization of a new full length <it>TMPRSS3 </it>isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

    Characterization of a new full length <it>TMPRSS3 </it>isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan oleh Shotland Lawrence I, Ploplis Barbara, MacLaren Linda, Dhillon Kiran, Luscombe Sandra, Ahmad Zahoor, Ramzan Khushnooda, Young Terry-Lynn, Riazuddin Saima, Powell Shontell D, Cindy Li Xiaoyan, Ahmed Zubair M, Ives Elizabeth, Riazuddin Sheikh, Friedman Thomas B, Morell Robert J, Wilcox Edward R

    Diterbitkan 2004-09-01
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