A new β-thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb08012.x/fullpdf
Reference7 articles.
1. α-Thalassemia DUE toframeshifts at Codons 5, 6, 8, and 8/9; Hematological Observations in Heterozygotes
2. Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114
3. A New β-Thalassemia Mutation Produced by a Single Nucleotide Substitution in the Conserved Dinucleotide Sequence of the IVS-I Consensus Acceptor Site (Ag→AA)
4. Molecular characterization of β-thalassemia mutations in Egypt
5. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
Cited by 6 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. Spectrum of β-Thalassemia Mutations in Egypt;Hemoglobin;1999-01
2. The β-and -Thalassemia Repository (Ninth Edition; Part I);Hemoglobin;1998-01
3. The β- and δ-Thalassemia Repository (Eighth Edition);Hemoglobin;1995-01
4. Organization of the human CD40L gene: implications for molecular defects in X chromosome-linked hyper-IgM syndrome and prenatal diagnosis.;Proceedings of the National Academy of Sciences;1994-03-15
5. The β- and δ-Thalassemia Repository (Seventh Edition);Hemoglobin;1993-01
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