Hb G-CHINESE: A G → C SUBSTITUTION AT CODON 30 OF THE α2-GLOBIN GENE CREATES APstI CUTTING SITE-Reference-Cited by-同舟云学术

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Hb G-CHINESE: A G → C SUBSTITUTION AT CODON 30 OF THE α2-GLOBIN GENE CREATES APstI CUTTING SITE

Published:2002-01 Issue:1 Volume:26 Page:95-97
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Chang Jan-Gowth,Shih Mu-Chin,Liu Su-Ching,Chen Chih-Mei,Chan Wen-Ling,Peng Ching-Tien

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-120002948

Reference4 articles.

1. An Abnormal Hæmoglobin in a Chinese: Hæmoglobin G

2. A New Hæmoglobin Variant (the ‘Honolulu Type’) in a Chinese

3. A Chemical Abnormality in Hemoglobin G from Chinese Individuals

4. Hb siriraj: A G→A substitution at codon 7 of the β-globin chain creates anMboll cutting site

Cited by 5 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 value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype–genotype correlation;Journal of Human Genetics;2021-10-25

2. 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

3. Three cases of the hemoglobin G-Chinese variant detected in patients of southern Chinese origin;Molecular Medicine Reports;2010-04-01

4. Hematological features and molecular lesions of hemoglobin gene disorders in Taiwanese patients;International Journal of Laboratory Hematology;2010-02

5. Association of Hb G‐Chinese [α30(B11)Glu→Gln] with α‐Thalassemia‐1 of the Thai Type in a Taiwanese Family;Hemoglobin;2003-01

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