Showing 1 - 8 results of 8 for search 'Safeer Ahmad', query time: 0.02s
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Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans by Muhammad Muzammal, Sana Fatima, Aisha Gul, Junaid Qayum, Arshad Farid, Safeer Ahmad, Wasim Shah, Muzammil Ahmad Khan
Published 2023-12-01
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Identification of a novel protein truncating mutation p.Asp98* in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family by Muhammad Z. Ali, Jasmin Blatterer, Muzammil A. Khan, Erich Schaflinger, Erwin Petek, Safeer Ahmad, Ejazullah Khan, Christian Windpassinger
Published 2020-02-01
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Identification of <i>GLI1</i> and <i>KIAA0825</i> Variants in Two Families with Postaxial Polydactyly by Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, Amjad Ullah Khan, Muhammad Ikram, Mari Muurinen, Shabir Hussain, Petra Loid, Muzammil Ahmad Khan, Outi Mäkitie
Published 2023-04-01
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Enhanced energy storage properties of La3+ modified 0.92Bi0.5Na0.5TiO3 -0.06Ba(Zr0.2Ti0.8)O3-0.02NaNbO3 ternary ceramic system by Aqib Ali Khan, Safeer Ahmad Arbab, Abdul Manan, Abdul Saboor, Atta Ullah, Noor Saeed Khattak, Iftikhar Ahmad, Muhammad Naeem Khan, Tariq Bashir, Muhammad Asif, Muhammad Sadiq, Muhammad Arif
Published 2021-01-01
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In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human <i>SLITRK1</i> Gene by Muhammad Zeeshan Ali, Arshad Farid, Safeer Ahmad, Muhammad Muzammal, Mohammed Al Mohaini, Abdulkhaliq J. Alsalman, Maitham A. Al Hawaj, Yousef N. Alhashem, Abdulmonem A. Alsaleh, Eman M. Almusalami, Mahpara Maryam, Muzammil Ahmad Khan
Published 2022-04-01
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A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family by Safeer Ahmad, Muhammad Zeeshan Ali, Sumra Wajid Abbasi, Safdar Abbas, Iftikhar Ahmed, Shakil Abbas, Shoaib Nawaz, Mubarak Ziab, Ikhlak Ahmed, Khalid A. Fakhro, Khalid A. Fakhro, Khalid A. Fakhro, Muzammil Ahmad Khan, Ammira Al-Shabeeb Akil, Ammira Al-Shabeeb Akil
Published 2023-03-01
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