A β-thalassemia ledon abolishes the sameMstII site as the sickle mutation
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/11/22/7789/7048644/11-22-7789.pdf
Cited by 28 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. Theme-Based Instruction: Making Conceptual Ties with the Sickle Cell Story;The American Biology Teacher;2010-09-01
2. The role of heterocellular hereditary persistence of fetal haemoglobin in β0-thalassaemia intermedia;British Journal of Haematology;2001-09
3. Rapid diagnosis of β thalassemia mutations in mediterraneans by PCR and restriction analysis of natural or created sites;Clinical Biochemistry;1997-07
4. Molecular Defects in Beta-Thalassaemia in the Population of Saudi Arabia;Human Heredity;1995
5. Rapid Diagnosis Of Two β-Thalassemia Mutatlons: Frameshift Codon 5 (-CT) And Codon 6 (-A);Pediatric Hematology and Oncology;1994-01
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