Identification of a novel 44.6-kb deletion causing α0 -thalassemia in southern China-Reference-Cited by-同舟云学术

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Identification of a novel 44.6-kb deletion causing α0 -thalassemia in southern China

Published:2017-02-28 Issue:4 Volume:39 Page:e94-e97
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

Wang Y.¹²³,Liu C.¹²³,Zhang L.⁴,Du L.¹²³,Zhou W.⁴,Huang S.⁴,Liu L.¹²³,Yin A.¹²³^ORCID

Affiliation:

1. Medical Genetic Center; Guangdong Women and Children Hospital; Guangzhou Guangdong China

2. Maternal and Children Metabolic-Genetic Key Laboratory; Guangdong Women and Children Hospital; Guangzhou Guangdong China

3. Guangdong Thalassemia Diagnostic Center; Guangzhou Guangdong China

4. Translational Research Center; Guangdong Women and Children Hospital; Guangdong China

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12643/fullpdf

Reference11 articles.

1. The alpha-thalassemias;Piel;N Engl J Med,2014

2. The prevalence and spectrum of alpha and beta thalassemia in Guangdong Province: implications for the future health burden and population screening;Xu;J Clin Pathol,2004

3. The prevalence and molecular spectrum of alpha- and beta-globin gene mutations in 14,332 families of Guangdong Province, China;Yin;PLoS One,2014

4. Nonimmune hydrops fetalis diagnosed during the second half of pregnancy in Southern China;Liao;Fetal Diagn Ther,2007

5. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants;Siriratmanawong;Fetal Diagn Ther,2007

Cited by 7 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. The First Thai Case of Nondeletional HbH Disease Caused by Compound Heterozygosity for α-Thalassemia-1 Chiang Rai (-- ^CR ) Type Deletion with Hb Constant Spring;Hemoglobin;2024-08-23

2. Single-tube multiplex real-time PCR with EvaGreen and high-resolution melting analysis for diagnosis of α0-thalassemia--SEA,--THAI, and--CR type deletions;PLOS ONE;2023-11-06

3. Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion;Scientific Reports;2023-06-17

4. Development of molecular diagnostic platform for α⁰‐thalassemia 44.6 kb (Chiang Rai, ‐‐^CR) deletion in individuals with microcytic red blood cells across Thailand;Annals of Human Genetics;2023-01-29

5. Novel α0-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease;Hemoglobin;2020-07-03

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