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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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f8d1752025235103d2aeb9e9010a67
https://doi.org/10.3109/03630269.2013.785434
https://doi.org/10.3109/03630269.2013.785434
