Hemoglobin H disease: not necessarily a benign disorder

Author:

Chui David H. K.1,Fucharoen Suthat1,Chan Vivian1

Affiliation:

1. From the Department of Pathology and Molecular Medicine, McMaster University Faculty of Health Sciences, Hamilton, ON, Canada; Thalassemia Research Center, Institute of Science and Technology for Research and Development, Mahidol University, Salaya Campus, Puttamonthon, Nakornpathom, Thailand; and University Department of Medicine, University of Hong Kong and Queen Mary Hospital, Hong Kong, China.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference143 articles.

1. Molecular genetics of the human globin genes.;Forget,2001

2. Molecular mechanisms of α-thalassemia.;Higgs,2001

3. Clinical and laboratory features of the α-thalassemia syndromes.;Higgs,2001

4. Homozygous α-thalassaemia: clinical presentation, diagnosis and management. A review of 46 cases.;Liang;Br J Obstet Gynaecol.,1985

5. Hydrops fetalis caused by α-thalassemia: an emerging health care problem.;Chui;Blood.,1998

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