The Thalassemia Repository (Ninth Edition; Part II)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269809113144
Reference148 articles.
1. -GγAγ-thalassemia and γ-chain variants in chinese newborn babies
2. G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.
3. A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin
4. The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C---- G substitution at nucleotide -195 of the A gamma-globin gene
Cited by 15 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. A Novel β-Thalassemia Insertion/Frameshift Mutation Between Codons 77/78 (p.Leu78Profs*13 or HBB: c.235_236insC) Observed in a Family in Bangladesh;Hemoglobin;2017-11-02
2. Diagnostic pitfalls of less well recognized HbH disease;Blood Cells, Molecules, and Diseases;2015-12
3. Detection of a Rare Mutation in An Iranian Family: Codons 37/38/39 (7 bp Deletion);Hemoglobin;2009-12
4. A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases;Hemoglobin;2008-01
5. Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology;Clinical Chemistry;2002-12-01
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