Sickle Cell Disease in the Kurdish Population of Northern Iraq-Reference-Cited by-同舟云学术

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Sickle Cell Disease in the Kurdish Population of Northern Iraq

Published:2012-06-11 Issue:4 Volume:36 Page:333-342
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Al-Allawi Nasir A.S.,Jalal Sana D.,Nerwey Farida F.,Al-Sayan Galawezh O.O.,Al-Zebari Sahima S.M.,Alshingaly Awny A.,Markous Raji D.,Jubrael Jaladet M.S.,Hamamy Hanan

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.692344

Reference39 articles.

1. Sickle-cell disease

2. Frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in Basra

3. Frequency of haemoglobinopathies at premarital health screening in Dohuk, Iraq: implications for a regional prevention programme

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1. Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq;Hemoglobin;2024-01-02

2. Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq;Hemoglobin;2023-05-04

3. The Impact of the Coinheritance of Alpha Thalassemia and Hemoglobin F Concentration on Sickle Cell Disease;Pharmacophore;2023

4. Molecular characterization of HBB gene mutations in beta-thalassemia patients of Southern Iraq;Biomedicine;2022-11-14

5. Stroke and stroke prevention in sickle cell anemia in developed and selected developing countries;Journal of the Neurological Sciences;2021-08

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