Molecular characterization of β-globin gene mutations in patients with β-thalassaemia intermedia in South China
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1988.tb02494.x/fullpdf
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3. beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.
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1. Molecular characterization of /3-thalassaemia in Singaporean Chinese: Application to prenatal diagnosis;Journal of Paediatrics and Child Health;2008-03-10
2. Molecular defects in the β-globin gene identified in different ethnic groups/populations during prenatal diagnosis for β-thalassemia: a Malaysian experience;Clinical and Experimental Medicine;2004-12
3. Genetic Factors Affecting Clinical Severity in β-Thalassemia Syndromes;Journal of Pediatric Hematology/Oncology;2000-11
4. Molecular diagnosis of patients with β-thalassemia major in central Taiwan by amplified created restriction site analysis;Journal of Human Genetics;1998-12
5. β-Thalassämie in Deutschland: Molekulargenetik und klinischer Phänotyp in der zugewanderten und in der heimischen Bevölkerung;Klinische Pädiatrie;1997-07
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