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pro vyhledávání: '"Ruqaya Abbas"'
Autor:
Al Alawi Ahmed, Thabet Ahmed, Nabeel J. Al Moamen, Hassan Sanad, Shaikha Al Arrayed, Ruqaya Abbas, Fawzia Mahdi, Ebtihal Salman
Publikováno v:
Hemoglobin. 37:369-377
Silent β-thalassemia (β-thal) is a group of mutations affecting the β-globin gene that cannot be differentiated in heterozygote states from normal conditions by using conventional criteria for the diagnosis of β-thal trait. Here we report the exi
Autor:
Al Moamen, Nabeel1 nmohammed2@health.gov.bh, Thabet, Ahmed2, Al Hajeri, Amani3, Newton, Hema4, Mahdi, Fawzia4, Abbas, Ruqaya4, Sanad, Hasan5
Publikováno v:
Bahrain Medical Bulletin. Mar2021, Vol. 43 Issue 1, p322-326. 5p.