Add to ORKGwhich permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. There is large variation in the molecular genetics and clinical features of hemoglobinopathies in Iran. Studying structural variants of hemoglobin demonstrated that th
Background and Objective: Hemoglobinopathies are among the most prevalent genetic disorders worldwid...
Background and Objective: Hemoglobin D-Punjab is one of the variant of hemoglobin caused by a mutati...
Abstract: Healthy carriers of severe Hemoglobinopathies are usually asymptomatic and only efficientl...
There is large variation in the molecular genetics and clinical features of hemoglobinopathies in Ir...
Beta-thalassemia is a genetic disorder that is caused by variations in the beta-hemoglobin (HBB) gen...
Hemoglobinopathies are the most common single gene disorders worldwide with a considerable frequency...
Copyright © 2015 Mehrnoosh Khodaeian et al. This is an open access article distributed under the Cre...
Background : The hemoglobinopathies refer to a diverse group of inherited disorders characterized by...
Thalassemia is one of the most common single gene disorders worldwide. Nearly 80 to 90 million with ...
More than 900 hemoglobin (Hb) variants have been reported, and most variants are caused by mutations...
We developed a series of interrelated locus-specific databases to store all published and unpublishe...
Hemoglobinopathies are inherited blood disorders with an autosomal recessive pattern. We aimed to ev...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Licen...
Hemoglobinopathy is an important genetic problem affecting millions of world population. The new alt...
ABSTRACT Background and Objectives: Hemoglobinopathies are characterized by defects in ...
Background and Objective: Hemoglobinopathies are among the most prevalent genetic disorders worldwid...
Background and Objective: Hemoglobin D-Punjab is one of the variant of hemoglobin caused by a mutati...
Abstract: Healthy carriers of severe Hemoglobinopathies are usually asymptomatic and only efficientl...
There is large variation in the molecular genetics and clinical features of hemoglobinopathies in Ir...
Beta-thalassemia is a genetic disorder that is caused by variations in the beta-hemoglobin (HBB) gen...
Hemoglobinopathies are the most common single gene disorders worldwide with a considerable frequency...
Copyright © 2015 Mehrnoosh Khodaeian et al. This is an open access article distributed under the Cre...
Background : The hemoglobinopathies refer to a diverse group of inherited disorders characterized by...
Thalassemia is one of the most common single gene disorders worldwide. Nearly 80 to 90 million with ...
More than 900 hemoglobin (Hb) variants have been reported, and most variants are caused by mutations...
We developed a series of interrelated locus-specific databases to store all published and unpublishe...
Hemoglobinopathies are inherited blood disorders with an autosomal recessive pattern. We aimed to ev...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Licen...
Hemoglobinopathy is an important genetic problem affecting millions of world population. The new alt...
ABSTRACT Background and Objectives: Hemoglobinopathies are characterized by defects in ...
Background and Objective: Hemoglobinopathies are among the most prevalent genetic disorders worldwid...
Background and Objective: Hemoglobin D-Punjab is one of the variant of hemoglobin caused by a mutati...
Abstract: Healthy carriers of severe Hemoglobinopathies are usually asymptomatic and only efficientl...