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pro vyhledávání: '"Nada Mohammed Alsharif"'
Autor:
Walaa Khalid Abulola, Rahaf Salah Osman Ahmad, Ebtehag Faham Alsulami, Nada Mohammed Alsharif, Adilah Hamoud Alturaifi, Abdulmajeed Aboud Alotaibi, Yasmen Taha Maimani
Publikováno v:
The Egyptian Journal of Hospital Medicine. 70:1880-1886
Background: Sickle cell disease (SCD) is an autosomal recessive disorder characterized by production of abnormal hemoglobin S, and it is associated with high morbidity and mortality. The highest prevalence of SCD in Saudi Arabia is in the Eastern pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5aff66fb6f1381e9df239d4b554da69
https://doi.org/10.12816/0044836
https://doi.org/10.12816/0044836
