Frequency of common <it>HFE </it>variants in the Saudi population: a high throughput molecular beacon-based study by Al-Hamed Mohamed, Al-Kayal Fadi, Alsmadi Osama A, Meyer Brian F

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Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi population by Rashed Mohammed S, Alsmadi Osama A, Imtiaz Faiqa, Al-Sayed Moeenaldeen, Meyer Brian F

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Weak or no association of <it>TCF7L2 </it>variants with Type 2 diabetes risk in an Arab population by Al-Daghri Nasser, Al-Saud Nouran, Al-Saud Haya, Alkayal Fadi, Mohamed Gamal, Al-Rubeaan Khalid, Alsmadi Osama, Mohammad Shahinaz, Meyer Brian F

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Molecular analysis of T^-B^-NK⁺severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia by Al-Kayal Fadi, Al-Saud Bandar, Al-Dhekri Hasan, Arnaout Rand, Al-Muhsen Saleh, Al-Ghonaium Abdulaziz, Alsmadi Osama, Al-Saud Haya, Al-Mousa Hamoud

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