Sickle Cell Disease in Jordan: The Experience of a Major Referral Center

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 lacking. AIM: To determine the genotypes responsib...

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Detalles Bibliográficos
Autores principales: Oudat, Raida I., Abualruz, Heba S., Al-Shiek, Nazih KH. Abu, AL-Mashaqba, Eman A., AL-Hiari, Rawan A., Alsoukhni, Hala A., Hammad, Ma’mon A. Abu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2021
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116085/
https://www.ncbi.nlm.nih.gov/pubmed/34012195
http://dx.doi.org/10.5455/medarh.2021.75.27-30

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116085/
https://www.ncbi.nlm.nih.gov/pubmed/34012195
http://dx.doi.org/10.5455/medarh.2021.75.27-30

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