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Nawaz, Hamed, Mujahid, , Khan, Sher Alam, Bibi, Farhana, Waqas, Ahmed ORCID: 0000-0002-3772-194X, Bari, Abdul, Fardous, , Khan, Niamatullah, Muhammad, Nazif, Khan, Amjad et al (show 10 more authors) , Paracha, Sohail Aziz, Alam, Qamre M, Kamal, Mohammad Azhar, Rafeeq, Misbahuddin, Muhammad, Noor, Ul Haq, Fayaz, Khan, Shazia, Mahmood, Arif, Khan, Saadullah and Umair, Muhammad (2023) Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome. GENES, 14 (5). 1113-.

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Waqas, Ahmed ORCID: 0000-0002-3772-194X, Nayab, Anam, Shaheen, Shabnam, Abbas, Safdar, Latif, Muhammad, Rafeeq, Misbahuddin M, Al-Dhuayan, Ibtesam S, Alqosaibi, Amany I, Alnamshan, Mashael M, Sain, Ziaullah M et al (show 4 more authors) , Habib, Alaa Hamed, Alam, Qamre, Umair, Muhammad and Saqib, Muhammad Arif Nadeem (2022) Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability. FRONTIERS IN GENETICS, 13. 878274-.