The β-thalassemias, including the hemoglobin E disorders, are not only common in the
Mediterranean region, South-East Asia, the Indian subcontinent and the Middle East but …

Objectives To investigate the mutational spectrum in the HBB gene in Arab patients with β-
thal. Methods Authors searched five databases (PubMed, Science Direct, Scopus, Web of …

β-Thalassemia is the most common hereditary disease in Iran. More than two million carriers
of β-thalassemia live in Iran. Since the Iranian population is a mixture of different ethnic …

In this report we describe the molecular analysis of 795 chromosomes derived from
unrelated Turkish β‐thalassemia and sickle cell anemia carriers identified in hematology …

Iran with an area of 1.648 million km2 is located between the Caspian Sea and the Persian
Gulf. The Iranian population consists of multiethnic groups that have been influenced by …

Background: Type 1 diabetes mellitus (DM) is a frequent complication in patients with beta‐
thalassemia. It is believed to be due to the damage inflicted by iron overload of the …

Objectives: β-Thalassemia disease is caused by mutations in the β-globin gene. This is
considered as one of the common genetic disorders in Syria. The aim of this study was to …

The spectrum of the β-thalassemia mutations of Thailand, Pakistan, India, Sri Lanka,
Mauritius and Syria has been further characterized by a multi-center study of 1,235 …

OBJECTIVES: The aim of this study was to update the incidence data of beta thalassaemia
mutations in various populations and compare it to the spectrum of mutations in the United …

β-Thalassemia (thal) is one of the most common genetic disorders in Iran and other
countries. Getting information on the distribution of mutations in different ethnic groups of …