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

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Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi A... von Hussein, Ibtessam Ramzi, Chaudhary, Adeel G, Bassiouni, Randa, AlQuaiti, Maha, Sogaty, Samira, Al-Qahtani, Mohammed

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An SP1-binding site polymorphism in the COLIAI gene and osteoporosis in Egyptian patients with thalassemia major von Hamed, Hanan M, Galal, Ashraf, Ghamrawy, Mona EL, Abd El Azeem, Khaled, Hussein, Ibtessam Ramzi, Abd-Elgawad, Mona Fayez

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The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families von 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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