Search Results - Rubina Dad

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  1. 1

    Rett Syndrome without MECP2 Mutation in a Pakistani Girl by Rubina Dad, Humaira Aziz Sawal, Arsalan Ahmad, Muhammad Ikram Ullah, Muhammad Jawad Hassan

    Published in Life and Science (2020-04-01)
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  2. 2

    Novel ATOH7 mutation and structural characterization in families with optic nerve hypoplasia by Muhammad Ikram Ullah, Rubina Dad, Zaira Rehman, Muhammad Shakil, Abdullah Alsrhani, Ayman Ali Mohammed Alameen, Heba Bassiony Ghanem, Emad Manni, Muhammad Umer Khan, Muhammad Atif

    Published in International Journal of Ophthalmology (2025-09-01)
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  3. 3

    Identification and Functional Characterization of Mutation in <i>FYCO1</i> in Families with Congenital Cataract by Muhammad Ikram Ullah, Zaira Rehman, Rubina Dad, Abdullah Alsrhani, Muhammad Shakil, Heba Bassiony Ghanem, Ayman Ali Mohammed Alameen, Mohamed Farouk Elsadek, Lienda Bashier Eltayeb, Sajjad Ullah, Muhammad Atif

    Published in Life (2023-08-01)
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