Search Results - Khalidah Khalid Nasser

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  1. 1
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    Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease by Haifa Mansour, Haifa Mansour, Babajan Banaganapalli, Babajan Banaganapalli, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Yousuf Al-Aama, Jumana Yousuf Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Omar Ibrahim Saadah, Omar Ibrahim Saadah, Ramu Elango, Ramu Elango

    Published 2022
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    Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families by Omar I. Saadah, Omar I. Saadah, Babajan Banaganapalli, Babajan Banaganapalli, Naglaa M. Kamal, Naglaa M. Kamal, Ahmed N. Sahly, Ahmed N. Sahly, Hadeel A. Alsufyani, Arif Mohammed, Aftab Ahmad, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Ramu Elango, Ramu Elango

    Published 2021
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