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pro vyhledávání: '"Heba S Abualruz"'
Autor:
Raida Oudat, Hala A Alsoukhni, Rawan A Al-Hiari, Heba S Abualruz, Eman A Al-Mashaqba, Ma'mon Abu Hammad, Nazih Kh Abu Al-Shiek
Publikováno v:
Medical Archives
Introduction Sickle cell disorders are the most frequently encountered hemoglobin variants in Jordan. Both alpha and beta thalassemias are also prevalent in this population. However, studies on the interaction between these hemoglobin disorders are l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::304e2400d4f3e7538dc76cff7c5ce63d
http://europepmc.org/articles/PMC8116085
http://europepmc.org/articles/PMC8116085
