Molecular Diagnosis of Fragile X Syndrome Using Methylation Sensitive Techniques in a Cohort of Patients With Intellectual Disability by Chaudhary, Adeel G., PhD, Hussein, Ibtessam R., MD PhD, Abuzenadah, Adel, PhD, Gari, Mamdouh, PhD, Bassiouni, Randa, MD, PhD, Sogaty, Samira, MBBCh, Lary, Sahira, PhD, Al-Quaiti, Maha, MSc, Al Balwi, Mohammed, PhD, Al Qahtani, Mohammed, PhD

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Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure by Al-Hussaini, Abdulrahman, MD, Faqeih, Eissa, MD, El-Hattab, Ayman W., MD, Alfadhel, Majid, Asery, Ali, MD, Alsaleem, Badr, MD, Bakhsh, Eman, MD, Ali, Ashraf, MD, Alasmari, Ali, MD, Lone, Khurram, MD, Nahari, Ahmed, MD, Eyaid, Wafaa, MD, Al Balwi, Mohammed, MD, Craig, Kate, PhD, Butterworth, Anna, BSc, He, Langping, PhD, Taylor, Robert W., PhD, FRCPath

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