βSglobin gene haplotype and the stroke risk among Egyptian children with sickle cell disease-Reference-Cited by-同舟云学术

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βSglobin gene haplotype and the stroke risk among Egyptian children with sickle cell disease

Published:2017-11-20 Issue:6 Volume:23 Page:362-367
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Abou-Elew Heba H.¹^ORCID,Youssry Ilham²^ORCID,Hefny Shireen³,Hashem Rania H.⁴,Fouad Nevine¹,Zayed Rania A.¹^ORCID

Affiliation:

1. Clinical and Chemical Pathology Department, Faculty of Medicine, Cairo University, Cairo, Egypt

2. Pediatric Department, Faculty of Medicine, Cairo University, Cairo, Egypt

3. Ministry of Health and population, Cairo, Egypt

4. Radiology Department Faculty of Medicine, Cairo University, Cairo, Egypt

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10245332.2017.1403736

Reference40 articles.

1. Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?

2. Atypical ?s haplotypes are generated by diverse genetic mechanisms

3. Bantu βs cluster haplotype predominates among Brazilian Blacks

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1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18

2. Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease;Genes;2023-10-09

3. Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon;Human Molecular Genetics;2023-02-08

4. High level of heterozygous haplotype of hemoglobin in Abidjan population with mild malaria;BMC Medical Genomics;2022-05-23

5. Protocol for “Genetic composition of sickle cell disease in the Arab population: A systematic review”;Health Science Reports;2022-05

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