Molecular Characterization of β-Thalassemia in Nineveh Province Illustrates the Relative Heterogeneity of Mutation Distributions in Northern Iraq
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-014-0369-1.pdf
Reference26 articles.
1. Weatherall DJ, Clegg JB (2001) The thalassaemia syndromes, 4th edn. Blackwell, Oxford
2. Galanello R, Origa R (2010) Beta-thalassemia. Orphanet J Rare Dis 5:11. doi: 10.1186/1750-1172-5-11
3. Hamamy H, Al-Allawi N (2013) The epidemiology of haemoglobinopathies in Arab countries. J Commun Genet 4:147–167
4. Tadmouri GO, Nair P, Obeid T, Al-Ali MT, Hamamy HA (2009) Consanguinity and reproductive health among Arabs. Reprod Health 6:17. doi: 10.1186/1742-4755-6-17
5. http://www.britannica.com/EBcheched/topic/376828/history-of-Mesopotamia
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3. Updated Molecular Spectrum of β-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration;Hemoglobin;2021-07-04
4. Genetic epidemiology of hemoglobinopathies among Iraqi Kurds;Journal of Community Genetics;2020-11-22
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