The Importance and Deficiencies of Medical Treatment Guidelines for Genetic Disorders in the Middle East Region by Majid alfadhel

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Artificial Intelligence in Genomic Analysis: Revolutionizing Healthcare by Majid Alfadhel

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P768: Congenital myopathy and split-foot malformation: A unique case without mesoaxial polydactyly by Muhammad Umair, Majid Alfadhel

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Caring for patients with rare diseases during the COVID-19 pandemic by Mohamed Boudjelal, Nimer Mehyar, Bandar Alghanem, Faisal Almajed, Majid Alfadhel

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Opinion of geneticist regarding performing preimplantation genetic testing for monogenic disorder for variants of unknown significance by Reema Alduaiji, Laila Alqahtani, Reema Alqadiri, Lena Alotaibi, Mostafa abolfotouh, Majid Alfadhel

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A nationwide cross-sectional study in Saudi Arabia for the assessment of understanding and practices of clinicians towards personalized genetic testing by Mohy Uddin, Ahmad Deeb, Husam Ardah, Marwan Nashbat, Mohammad Yahya Ayoub, Majid Alfadhel

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Common disease-associated gene variants in a Saudi Arabian population by Mariam Aleissa, Taghrid Aloraini, Lamia Fahad Alsubaie, Madawi Hassoun, Ghada Abdulrahman, Abdulrahman Swaid, Wafa Al Eyaid, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, Ahmed Alfares

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Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome) by Majid Alfadhel, Bashayr S. Alhubayshi, Muhammad Umair, Ahmed Alfaidi, Deemah Alwadaani, Essra Aloyouni, Safdar Abbas, Abdulkareem Al Abdulrahman, Mohammed Aldrees, Abeer Al Tuwaijri, Ruaa S. Alharithy, Abdulaziz Alajlan, Abdulrahman Alswaid, Saad Almohrij, Sultan Al-Khenaizan

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Clinical and molecular characterization of hepatic glycogen storage disease in Saudi Arabia by Abdulrahman Al-Hussaini, Mohammed AlMannai, Muhannad Alruwaithi, Eissa Faqeih, Ali Alasmari, Majid Alfadhel, Fuad Al Mutairi, Mohammed Saleh, Abdullah AlZaben, Yaser Alobailan, Moodhi Alharbi, Manal AlAfqi, Alaa Alayed, Abdul Ali Peer-Zada, Yasir Alrusayni

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Clinical and molecular characterization of hepatic glycogen storage disease in Saudi Arabia. by Abdulrahman Al-Hussaini, Mohammed AlMannai, Muhannad Alruwaithi, Eissa Faqeih, Ali Alasmari, Majid Alfadhel, Fuad Al Mutairi, Mohammed Saleh, Abdullah AlZaben, Yaser Alobailan, Moodhi Alharbi, Manal AlAfqi, Alaa Alayed, Abdul Ali Peer-Zada, Yasir Alrusayni

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