Homozygosity for the Mediterranean α-thalassemic deletion (hemoglobin Barts hydrops fetalis)-Reference-Cited by-同舟云学术

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Homozygosity for the Mediterranean α-thalassemic deletion (hemoglobin Barts hydrops fetalis)

Published:2010-03 Issue:2 Volume:30 Page:153-155
ISSN:0256-4947
Container-title:Annals of Saudi Medicine
language:en
Short-container-title:Annals of Saudi Medicine

Author:

Al-Allawi Nasir A. S.¹,Shamdeen Maida Y.²,Rasheed Najeeb S.³

Affiliation:

1. From the Department of Pathology, College of Medicine, University of Dohuk, Dohuk, Iraq

2. From the Department of Gynecology and Obstetrics, College of Medicine, University of Dohuk, Dohuk, Iraq

3. From the Department of Hematology, Azadi Teaching Hospital, Dohuk, Iraq

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

Reference12 articles.

1. Rapid detection of common Mediterranean α-globin deletions/rearrangements using PCR;Oron-Karni V;Am J Hematol,1998

2. The α-globin gene cluster, genetics and disorders;Waye JS;Clin Invest Med,2001

3. The Thalassaemia Syndromes

4. A review of the molecular genetics of the human α-globin gene cluster;Higgs DR;Blood,1989

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1. Genetic epidemiology of hemoglobinopathies among Iraqi Kurds;Journal of Community Genetics;2020-11-22

2. Molecular analysis of a large novel deletion causing α+-thalassemia;BMC Medical Genetics;2019-05-06

3. Detection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family;Hemoglobin;2019-03-04

4. Characterization of Hb Bart’s Hydrops Fetalis Caused by – –SEAand a Large Novel α0-Thalassemia Deletion;Hemoglobin;2018-01-02

5. In Utero Transfer of Adeno-Associated Viral Vectors Produces Long-Term Factor IX Levels in a Cynomolgus Macaque Model;Molecular Therapy;2017-08

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