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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Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability by Karim, Sajjad, Hussein, Ibtessam Ramzi, Schulten, Hans-Juergen, Alsaedi, Saad, Mirza, Zeenat, Al-Qahtani, Mohammed, Chaudhary, Adeel

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