Hasil Pencarian - Muhammad Azhar Baig

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  1. 1
    P.arg102ser is a common Pde6? mutation causing autosomal recessive retinitis pigmentosa in Pakistani families

    P.arg102ser is a common Pde6? mutation causing autosomal recessive retinitis pigmentosa in Pakistani families oleh Anosha Ali Khan, Yar Muhammad Waryah, Muhammad Iqbal, Hafiz Muhammad Azhar Baig, Muhammad Rafique, Ali Muhammad Waryah

    Diterbitkan 2020-11-01
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  2. 2
    Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

    Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder oleh Francesca Mattioli, Hossein Darvish, Sohail Aziz Paracha, Abbas Tafakhori, Saghar Ghasemi Firouzabadi, Marjan Chapi, Hafiz Muhammad Azhar Baig, Alexandre Reymond, Stylianos E. Antonarakis, Muhammad Ansar

    Diterbitkan 2021-11-01
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  3. 3
    Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients

    Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients oleh Yar Muhammad Waryah, Muhammad Iqbal, Shakeel Ahmed Sheikh, Muhammad Azhar Baig, Ashok Kumar Narsani, Muhammad Atif, Munir Ahmad Bhinder, Attiq Ur Rahman, Azam Iqbal Memon, Muhammad Suleman Pirzado, Ali Muhammad Waryah

    Diterbitkan 2019-01-01
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