Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi β-Thalassemia Patients by Alsaleem, Hassan, Alzahrani, Alhusain J., Steinberg, Martin H., Ali, Amein K. Al, Sulaiman, Ahmed, Jarrash, Sana Al, Nasserullah, Zaki A., Chathoth, Shahanas, Al-Rubaish, Abdullah, Borgio, J. Francis, Vatte, Chittibabu, Cyrus, Cyril, Qutub, Hatem

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Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi [beta]-Thalassemia Patients by Cyrus, Cyril, Vatte, Chittibabu, Borgio, J. Francis, Rubaish, Abdullah Al, Chathoth, Shahanas, Nasserullah, Zaki A, Jarrash, Sana Al, Sulaiman, Ahmed, Qutub, Hatem, Alsaleem, Hassan, Alzahrani, Alhusain J, Steinberg, Martin H, Ali, Amein K. Al

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Demands and challenges for patients with sickle-cell disease requiring hematopoietic stem cell transplantation in Saudi Arabia by Alsultan, Abdulrahman, Jastaniah, Wasil, Al Afghani, Sameera, Al Bagshi, Muneer H., Nasserullah, Zaki, Al-Suliman, Ahmed M., Alabdulaali, Mohammed K.

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Spectrum of α-Thalassemia Mutations in Transfusion-Dependent β-Thalassemia Patients from the Eastern Province of Saudi Arabia by Akhtar, Mohammed Shakil, Qaw, Fuad, Borgio, J. Francis, Albuali, Waleed, Suliman, Ahmed, Nasserullah, Zaki, Al-Jarrash, Sana, Al-Ali, Amein

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Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-[beta]0 thalassemia by Alsultan, Abdulrahman, Ngo, Duyen, Bae, Harold, Sebastiani, Paola, Baldwin, Clinton T, Melista, Efthymia, Suliman, Ahmed M, Albuali, Waleed H, Nasserullah, Zaki, Luo, Hong-yuan, Chui, David H.K, Steinberg, Martin H, Al-Ali, Amein K

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Genetic studies of fetal hemoglobin in the Arab‐Indian haplotype sickle cell‐β 0 thalassemia by Alsultan, Abdulrahman, Ngo, Duyen, Bae, Harold, Sebastiani, Paola, Baldwin, Clinton T., Melista, Efthymia, Suliman, Ahmed M., Albuali, Waleed H., Nasserullah, Zaki, Luo, Hong‐yuan, Chui, David H.K., Steinberg, Martin H., Al‐Ali, Amein K.

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Genetic studies of fetal hemoglobin in the Arab‐Indian haplotype sickle cell‐β0 thalassemia by Alsultan, Abdulrahman, Ngo, Duyen, Bae, Harold, Sebastiani, Paola, Baldwin, Clinton T., Melista, Efthymia, Suliman, Ahmed M., Albuali, Waleed H., Nasserullah, Zaki, Luo, Hong‐yuan, Chui, David H.K., Steinberg, Martin H., Al‐Ali, Amein K.

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Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia by Alsultan, Abdulrahman, Ngo, Duyen, Bae, Harold, Sebastiani, Paola, Baldwin, Clinton T, Melista, Efthymia, Suliman, Ahmed M, Albuali, Waleed H, Nasserullah, Zaki, Luo, Hong-Yuan, Chui, David H K, Steinberg, Martin H, Al-Ali, Amein K

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Regional experience with newborn screening for sickle cell disease, other hemoglobinopathies and G6PD deficiency by Nasserullah, Zaki, Alshammari, Ali, Abbas, Marriam Al, Abu-Khamseen, Yousef, Qadri, Mohamed, Jafer, Souad Al, Wabel, Manal Al

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The effect of alpha-thalassemia on cord blood red cell indices and interaction with sickle cell gene by Quadri, M I, Islam, S I, Nasserullah, Z

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Neonatal Screening for Sickle Cell Disease, Glucose-6-Phosphate Dehydrogenase Deficiency and α-Thalassemia in Qatif and Al Hasa by Nasserullah, Zaki, Al Jame, Abdulaziz, Abu Srair, Hussain, Al Qatari, Ghazi, Al Naim, Saad, Al Aqib, Amin, Mokhtar, Mohamed

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