PRENATAL DIAGNOSIS OF β-THALASSEMIA IN EGYPT: Implementing Accurate High-Tech Methods Did not Reflect Much on the Outcome-Reference-Cited by-同舟云学术

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PRENATAL DIAGNOSIS OF β-THALASSEMIA IN EGYPT: Implementing Accurate High-Tech Methods Did not Reflect Much on the Outcome

Published:2008-01 Issue:6 Volume:25 Page:541-548
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Elgawhary S.,Elbaradie Sahar M. Y.,Rashad Wael M.,Mosaad Maha,Abdalla M. A. H.,Ezzat G.,Wali Yassar A.,Elbeshlawy A.

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1080/08880010802313509

Reference20 articles.

1. Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state

2. An Egyptian β-thalassaemia heterozygote with normal haemoglobins A2 and F: A problem in population screening

3. Rapid Screening of Multiple β-Globin Gene Mutations by Real-Time PCR on the LightCycler: Application to Carrier Screening and Prenatal Diagnosis of Thalassemia Syndromes

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genomics in Egypt: Current Status and Future Aspects;Frontiers in Genetics;2022-05-13

2. Prevalence of iron deficiency anemia and beta thalassemia carriers among relatives of beta thalassemia patients in Nile Delta region, Egypt: a multicenter study;Journal of the Egyptian Public Health Association;2021-10-11

3. Cultural Preferences and Limited Public Resources Influence the Spectrum of Thalassemia in Egypt;Journal of Pediatric Hematology/Oncology;2015-05

4. Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients;Egyptian Journal of Medical Human Genetics;2015-04

5. The first five years of a preventive programme for haemoglobinopathies in Northeastern Iraq;Journal of Medical Screening;2013-10-21

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