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Hemoglobin
international journal for hemoglobin research
Volume 38, 2014 - Issue 1
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Research Article

The Hb H Disease Genotypes in Southern China

Jianpei FangDepartment of Pediatrics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University GuangzhouPeople’s Republic of China
,
Luming ChenDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of China
,
Ruiping ZengDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of China
,
Qiuhong TianDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of China
,
Weiying JiangDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of China
,
Hongyi LiDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of China
,
Zheng ChenDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of China
,
Chuanshu DuDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of China
&
Suqin ChenDepartment of Medical Genetics, Zhongshan Medical College, Sun Yat-sen University GuangzhouPeople’s Republic of ChinaCorrespondence[email protected]
 show all
Pages 76-78 | Received 24 May 2013, Accepted 13 Jul 2013, Published online: 21 Nov 2013

Citations (11)

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Read on this site (5)

Shao-Min Wu, Su-Ran Huang, Chan Li, Gui-Lan Chen & Dong-Zhi Li. (2022) Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report. Hemoglobin 46:6, pages 341-343.
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Qiang Zhao, Su-Min Zhao, Xue Zhang, Shi-Ping Chen, Jun Sun, Zhi-Yu Peng, Yan Sun, Chuang Fan, Xiao-Dan Xing & Rong Li. (2021) Detection of the HBB: c.393T>G Mutation in Two Patients with Hypochromic Microcytic Anemia. Hemoglobin 45:3, pages 150-153.
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Hua Jiang, Lv-Yin Huang, Li Zhen, Fan Jiang & Dong-Zhi Li. (2017) Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease. Hemoglobin 41:4-6, pages 293-296.
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Xin Yang, Jin-Mei Yan, Jian Li, Xing-Mei Xie, Jian-Ying Zhou, Yan Li & Dong-Zhi Li. (2016) Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion. Hemoglobin 40:5, pages 353-355.
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Luhao Han, Hai Su, Hao Wu, Weiying Jiang & Suqin Chen. (2016) Molecular Epidemiological Survey of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassemia in Uygur and Kazak Ethnic Groups in Xinjiang, Northwest China. Hemoglobin 40:3, pages 179-186.
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Articles from other publishers (6)

Feicui Zhang, Congcong Kong, Zhenmin Ma, Wenchao Chen, Yue Li, Heqiang Lou & Jiasheng Wu. (2023) Molecular characterization and transcriptional regulation analysis of the Torreya grandis squalene synthase gene involved in sitosterol biosynthesis and drought response. Frontiers in Plant Science 14.
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Li Du, Xiuqin Bao, Wei He, Danqing Qin, Jicheng Wang, Ying Xiong, Xiaomei Shi, Hongke Ding, Cuize Yao & Jing Wu. (2021) Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden ( HBA2 :c.178G>C) and Hb Quong Sze ( HBA2 :c.377T>C) . Journal of International Medical Research 49:7, pages 030006052110314.
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Chunxiu Lin, Yue Chen, Yizi Lin, Xuebei Wang, Lanyun Hu, Yong Cao & Yunjiao Chen. (2020) Antistress and anti-aging activities of Caenorhabditis elegans were enhanced by Momordica saponin extract. European Journal of Nutrition 60:4, pages 1819-1832.
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Prashant Sharma, Reena Das, Alka Rani Khadwal, Indrani Karmakar, Jasbir Kaur Hira & Sanjeev Chhabra. (2020) HbH disease due to compound heterozygosity for hemoglobins Zürich‐Albisrieden and Sallanches. Pediatric Blood & Cancer 67:4.
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Mostafa Paridar, Ebrahim Azizi, Bijan Keikhaei, Vahideh Takhviji, Iman Baluchi & Abbas Khosravi. (2019) Iranian patients with hemoglobin H disease: genotype–phenotype correlation. Molecular Biology Reports 46:5, pages 5041-5048.
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Qing Li, Juan Tang & Yi Ju. (2016) Effect of Hb H on HbA1c measurements as measured by IFCC reference method and affinity HPLC. Clinical Chemistry and Laboratory Medicine (CCLM) 54:8.
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