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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Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects by Hussein, Ibtessam R., Bader, Rima S., Chaudhary, Adeel G., Bassiouni, Randa, Alquaiti, Maha, Ashgan, Fai, Schulten, Hans-Juergen, Al Qahtani, Mohammad H.

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Application of molecular genetics techniques for detecting deleted segmental aneuploidy in Williams Syndrome by Magbooli, Afaf, Huwait, Etimad, Hussein, Ibtessam R, AlQahtani, Mohammed

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Characterization of familial breast cancer in Saudi Arabia by Merdad, Adnan, Gari, Mamdooh A, Hussein, Shireen, Al-Khayat, Shadi, Tashkandi, Hana, Al-Maghrabi, Jaudah, Al-Thubaiti, Fatma, Hussein, Ibtessam R, Koumosani, Taha, Shaer, Nehad, Chaudhary, Adeel G, Abuzenadah, Adel M, Al-Qahtani, Mohammed H, Dallol, Ashraf

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Detection of rare single nucleotide variants affecting genes in the DNA repair pathways in hereditary breast cancer by Hussein, Shireen, Merdad, Adnan, Al-Maghrabi, Jaudah, Gari, Mamdooh A, Al-Thubaiti, Fatma, Hussein, Ibtessam R, Chaudhary, Adeel G, Abuzenadah, Adel M, Tashkandi, Hanaa, Al-Khayyat, Shadi, Kumosani, Taha, Al-Qahtani, Mohammed H, Dallol, Ashraf

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Egyptian Society of Liver Cancer Recommendation Guidelines for the Management of Hepatocellular Carcinoma [Corrigendum] by Omar, Ashraf, Kaseb, Ahmed, Elbaz, Tamer, El-Kassas, Mohamed, El Fouly, Amr, Hanno, Abdel Fatah, El Dorry, Ahmed, Hosni, Ahmed, Helmy, Amr, Saad, Amr S, Alolayan, Ashwaq, Eysa, Basem, Hamada, Emad, Azim, Hamdy, Khattab, Hany, Elghazaly, Hesham, Tawfik, Hesham, Ayoub, Hisham, Khaled, Hussein, Saadeldin, Ibtessam, Waked, Imam, Barakat, Eman, El Meteini, Mahmoud, Hamed Shaaban, Mohamed, EzzElarab, Mohamed, Fathy, Mohamed, Shaker, Mohamed, Sobhi, Mohamed, Shaker, Mohamed, ElGharib, Mohamed, Abdullah, Mohammed, Mokhtar, Mohesn, Elshazli, Mostafa, Heikal, Omar, Hetta, Osama, ElWakil, Reda, Abdel Wahab, Sameh, Eid, Samir, Rostom, Yousri

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The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families by HUSSEIN, I. R., EL-BESHLAWY, A., SALEM, A., MOSAAD, R., ZAGHLOUL, N., RAGAB, L., FAYEK, H., GABER, K., EL-EKIABI, M.

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