A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies by Monies, Dorota, Alhindi, Hindi N, Almuhaizea, Mohamed A, Abouelhoda, Mohamed, Alazami, Anas M, Goljan, Ewa, Alyounes, Banan, Jaroudi, Dyala, AlIssa, Abdulelah, Alabdulrahman, Khalid, Subhani, Shazia, El-Kalioby, Mohamed, Faquih, Tariq, Wakil, Salma M, Altassan, Nada A, Meyer, Brian F, Bohlega, Saeed

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Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency by AlHarbi, Musa, Ali Mobark, Nahla, AlMubarak, Latifa, Aljelaify, Rasha, AlSaeed, Mariam, Almutairi, Amal, Alqubaishi, Fatmah, Hussain, M. Emarat, Balbaid, Ali Abdullah O., Said Marie, Amal, AlSubaie, Lamia, AlShieban, Saeed, alTassan, Nada, Ramkissoon, Shakti H., Abedalthagafi, Malak

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New insights into the genomic landscape of meningiomas identified FGFR3 in a subset of patients with favorable prognoses by AlSahlawi, Aysha, Aljelaify, Rasha, Magrashi, Amna, AlSaeed, Mariam, Almutairi, Amal, Alqubaishi, Fatimah, Alturkistani, Abdulellah, AlObaid, Abdullah, Abouelhoda, Mohamed, AlMubarak, Latifa, AlTassan, Nada, Abedalthagafi, Malak

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COVID-19 in Unvaccinated patients with inherited metabolic disorders: A single center experience by Altassan, Ruqaiah, Sulaiman, Raashda A., Alfalah, Abdullah, Alwagiat, Waad, Megdad, Eman, Alqasabi, Dana, Handoom, Bedour, Almesned, Munirah, Al-Amri, Hassan, Alhassnan, Zuhair, Alsayed, Moeen-aldeen, Alzaidan, Hamad, Rahbeeni, Zuhair, Derar, Nada, Al-Owain, Mohammed, Albanyan, Esam

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IMMU-01. DURABLE RESPONSE TO NIVOLUMAB IN A PEDIATRIC PATIENT WITH REFRACTORY GLIOBLASTOMA AND CONSTITUTIONAL BIALLELIC MISMATCH REPAIR DEFICIENCY by AlHarbi, Musa, Mobark, Nahla Ali, Al-Mubarak, Latifa, Alaljelaify, Rasha, AlSaeed, Mariam, Almutairi, Amal, Alqubaishi, Fatmah, Hussain, Emarat, AlSubaie, Lamia, AlShieban, Saeed, alTassan, Nada, Ramkissoon, Shakti H, Abedalthagafi, Malak

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HGG-03. PREVALENCE OF BIALLELIC MISMATCH REPAIR DEFICIENCY IN CHILDREN WITH MALIGNANT GLIOMA TREATED AT KING FAHAD MEDICAL CITY (KFMC) by Mobark, Nahla Ali, Mosleh, Othman, Marie, Amal Abd Al Samie, AlMubara, Latifa, AlTassan, Nada, Howakins, Cynthia, Alshammari, Faris Safaq Faris Safaq, Al-Huzaimi, Fatimah Ibrahim, Aboabat, Roba Ibrahim, AlDossari, Fay Saad, AlGhamdi, Ghaida Ali, Balbaid, Ali Abdullah O, Al-Harbi, Musa, Abedalthagafi, Malak

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Association of the angiotensinogen gene polymorphism with atherosclerosis and its risk traits in the Saudi population by Al-Najai, Mohammed, Muiya, Paul, Tahir, Asma I, Elhawari, Samar, Gueco, Daisy, Andres, Editha, Mazhar, Nejat, Altassan, Nada, Alshahid, Maie, Dzimiri, Nduna

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Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family by AlHarbi, Musa, Mubarak, Nahla, AlMubarak, Latifa, Aljelaify, Rasha, AlSaeed, Mariam, Almutairi, Amal, AlJabarat, Weal, Alqubaishi, Fatimah, Al-Subaie, Lamia, AlTassan, Nada, Neben, Cynthia L., Zhou, Alicia Y., Abedalthagafi, Malak

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The 3'-UTR of the adiponectin Q gene harbours susceptibility loci for atherosclerosis and its metabolic risk traits by Muiya, Nzioka, Al-Najai, Mohammed, Tahir, Asma I, Elhawari, Samar, Gueco, Daisy, Andres, Editha, Mazhar, Nejat, Altassan, Nada, Meyer, Brian F, Alshahid, Maie, Dzimiri, Nduna

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In silico analysis of influence of the missense mutation P629S on the molecular interaction and 3D properties of PIK3R5 by Shinwari, Jameela, Tahir, Asma I., Bohlega, Saeed, AlTassan, Nada

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Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family by AlHarbi, Musa, Mubarak, Nahla, AlMubarak, Latifa, Aljelaify, Rasha, AlSaeed, Mariam, Almutairi, Amal, AlJabarat, Weal, Alqubaishi, Fatimah, Al-Subaie, Lamia, AlTassan, Nada, Neben, Cynthia L, Zhou, Alicia Y, Abedalthagafi, Malak

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