Association of Hb G‐Chinese [α30(B11)Glu→Gln] with α‐Thalassemia‐1 of the Thai Type in a Taiwanese Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1081/HEM-120018435
Reference8 articles.
1. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions
2. Hb MANITOBA IN A TAIWANESE FAMILY: A C → A SUBSTITUTION AT CODON 102 OF THE α2-GLOBIN GENE
3. Hb siriraj: A G→A substitution at codon 7 of the β-globin chain creates anMboll cutting site
4. An Abnormal Hæmoglobin in a Chinese: Hæmoglobin G
5. Hb G-CHINESE: A G → C SUBSTITUTION AT CODON 30 OF THE α2-GLOBIN GENE CREATES APstI CUTTING SITE
Cited by 2 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. The First Case of Hb G-Honolulu [α30(B11)Glu→Gln (GAG>CAG); HBA2:c.91G>A] Observed in Association with Hb S [β6(A3)Glu→Val, GAG>GTG] in a Healthy Italian Child;Hemoglobin;2011-09-19
2. Three cases of the hemoglobin G-Chinese variant detected in patients of southern Chinese origin;Molecular Medicine Reports;2010-04-01
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