Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features

Journal article

Open access

Peer reviewed

American journal of hematology, Vol.96(4), pp.E117-E121

01/04/2021

PMID: 33460474

Abstract

Adolescent

Adult

Aged

Aged, 80 and over

alpha-Globins - genetics

alpha-Thalassemia - epidemiology

alpha-Thalassemia - genetics

Anemia, Sickle Cell - blood

Anemia, Sickle Cell - epidemiology

Anemia, Sickle Cell - genetics

beta-Globins - genetics

Child

Child, Preschool

Female

Fetal Hemoglobin - analysis

Haplotypes - genetics

Humans

Male

Middle Aged

Polymorphism, Single Nucleotide

Saudi Arabia - epidemiology

Sickle Cell Trait - epidemiology

Sickle Cell Trait - genetics

Tanzania - epidemiology

Young Adult

url

https://doi.org/10.1002/ajh.26096View

Published (Version of record) Open

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Title: Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features
Creators - without role: Amein K Al-Ali - King Faisal University
Ahmed Alsulaiman - King Faisal University
Mohammed Alfarhan - King Faisal University
Surinder Safaya - King Faisal University
Chitti Babu Vatte - Imam Abdulrahman Bin Faisal University
Waleed M Albuali - King Faisal University
Hatem O Qutub - King Faisal University
Alhusain J Alzahrani - University of Hafr Al-Batin
Jacqueline N Milton - Boston University
Martin H Steinberg - Boston Medical Center
Publication Details: American journal of hematology, Vol.96(4), pp.E117-E121
Identifiers: 9914490408331
Academic Unit: Hafr Albatin University; King Faisal University; Imam Abdulrahman Bin Faisal University
Language: English
Resource Type: Journal article