Early Onset of Fetal Hydrops Associated with the α-Thalassemia – –THAIDeletion
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2014.974609
Reference21 articles.
1. The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions
2. Carrier screening for ?- and ?-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital
3. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening
4. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions
Cited by 4 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. Hb Bart’s Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (– –CR) α0-Thalassemia in Two Unrelated Thai Families;Hemoglobin;2021-04-06
2. Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation ‐‐ SEA /‐‐ CR , a novel α 0 ‐thalassemia deletion;International Journal of Laboratory Hematology;2020-01-13
3. Molecular Spectrum of α- and β-Thalassemia Mutations in a Large Ethnic Hakka Population in Southern China;Hemoglobin;2018-03-04
4. Characterization of Hb Bart’s Hydrops Fetalis Caused by – –SEAand a Large Novel α0-Thalassemia Deletion;Hemoglobin;2018-01-02
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