Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-Thalassemia Codon 17 (A>T) in a Thai Patient
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.669358
Reference11 articles.
1. SYTO9 and SYBR Green1 with High Resolution Melting Analysis for Molecular Confirmatory Testing of the Common Southeast Asian β0-thalassemia Mutations
2. Detection of β-Thalassemia Mutations Using a Multiplex Amplification Refractory Mutation System Assay
3. SYTO9 and SYBR GREEN1 with a high-resolution melting analysis for prenatal diagnosis of β0-thalassemia/hemoglobin-E
4. Hemoglobinopathies in Southeast Asia
5. Interference of Hemoglobin Hope on β-Thalassemia Diagnosis by the Capillary Electrophoresis Method
Cited by 1 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. Hemoglobin Q-Thailand and its Combinations with other Forms of Thalassemia or Hemoglobinopathies in Northern Thailand;Clinical Laboratory;2014
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