The β-and -Thalassemia Repository (Ninth Edition; Part I)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269809092143
Reference184 articles.
1. Codon 4 ACT→ACA, codon 5 CCT→TCT, and codon 6 GAG→TAG mutations in cis position: A form of thalassemia trait
2. beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.
3. A novel β-thalassaemia mutation in the 5’untranslated region of the β-globin gene
4. β-Thalassemia resulting from a single nucleotide substitution in an acceptor splice site
Cited by 57 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. Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran;Hemoglobin;2019-01-02
2. The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran;Hemoglobin;2017-01-02
3. Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia;Clinical Chemistry and Laboratory Medicine (CCLM);2013-06-26
4. Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia;Clinical Chemistry and Laboratory Medicine (CCLM);2013-03-13
5. Prenatal diagnosis for thalassaemia in Egypt: what changed parents' attitude?;Prenatal Diagnosis;2012-06-13
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