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Hemoglobin
international journal for hemoglobin research
Volume 12, 1988 - Issue 5-6
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Original Article

Different Forms of Hb H Disease in the Chinese

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Pages 499-507 | Received 13 Nov 1967, Accepted 01 Jun 1988, Published online: 07 Jul 2009

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Jing Zhong Liu, Cai Ying Ou, Li Rong Wang, Bai Xiao, Li Jia Huang & Li Chang Chen. (2004) Detection of Three Common, Deletional α‐Thalassemia Determinants in Southern China by a Single‐Tube Multiplex Polymerase Chain Reaction Method. Hemoglobin 28:1, pages 39-44.
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J. S. Waye, B. Eng, M. Patterson, D. H.K. Chui, E. Nisbet-Brown & N. F. Olivieri. (1997) Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease. Hemoglobin 21:5, pages 469-472.
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Articles from other publishers (16)

Pacharapan Surapolchai, Ampaiwan Chuansumrit, Nongnuch Sirachainan, Praguywan Kadegasem, Ka-Chun Leung & Chi-Chiu So. (2017) A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease. Annals of Hematology 96:6, pages 1005-1014.
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Vichai Laosombat, Vip Viprakasit, Thirachit Chotsampancharoen, Malai Wongchanchailert, Sudarat Khodchawan, Worawut Chinchang & Benjamas Sattayasevana. (2009) Clinical features and molecular analysis in Thai patients with HbH disease. Annals of Hematology 88:12, pages 1185-1192.
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Jin Ai Mary Anne Tan, Juan Loong Kok, Kim Lian Tan, Yong Chui Wee & Elizabeth George. (2009) Thalassemia intermedia in HbH-CS disease with compound heterozygosity for .BETA.-thalassemia: Challenges in hemoglobin analysis and clinical diagnosis. Genes & Genetic Systems 84:1, pages 67-71.
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Suthat Fucharoen & Vip Viprakasit. (2009) Hb H disease: clinical course and disease modifiers. Hematology 2009:1, pages 26-34.
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D. Z. Li, C. Liao, J. Li, X. M. Xie, Y. N. Huang & Q. C. Wu. (2005) Hemoglobin H hydrops fetalis syndrome resulting from the association of the - -SEA deletion and the alphaQuong Szealpha mutation in a Chinese woman. European Journal of Haematology 75:3, pages 259-261.
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K. Y. Leung, C. P. Lee, M. H. Y. Tang, H. Y. Chan, E. S. K. Ma & V. Chan. (2004) Detection of increased middle cerebral artery peak systolic velocity in fetuses affected by hemoglobin H Quong Sze disease. Ultrasound in Obstetrics & Gynecology 23:5, pages 525-526.
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David H. K. ChuiSuthat FucharoenVivian Chan. (2003) Hemoglobin H disease: not necessarily a benign disorder. Blood 101:3, pages 791-800.
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S.K. Ma, A.Y.Y. Chan, E.K.W. Chiu & L.C. Chan. (2001) Haemoglobin H disease due to (- - SEA ) α-globin gene deletion and α2-codon 30 (ΔGAG) mutation: a family study . Clinical & Laboratory Haematology 23:5, pages 325-327.
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Fred Lorey, Pimlak Charoenkwan, H. Ewa Witkowska, John Lafferty, Margaret Patterson, Barry Eng, John S. Waye, Jerry Z. Finklestein & David H. K. Chui. (2001) Hb H hydrops foetalis syndrome: a case report and review of literature. British Journal of Haematology 115:1, pages 72-78.
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John S. Waye, Barry Eng, Margaret Patterson, Lynda Walker, Manuel D. Carcao, Nancy F. Olivieri & David H.K. Chui. (2001) Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases. American Journal of Hematology 68:1, pages 11-15.
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Frederick E. Chen, Clara Ooi, Sau Yin Ha, Bernard M.Y. Cheung, David Todd, Raymond Liang, Tai Kwong Chan & Vivian Chan. (2000) Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients. New England Journal of Medicine 343:8, pages 544-550.
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C.S. Chim, Vivian Chan & D. Todd. (1998) Hemosiderosis with diabetes mellitus in untransfused hemoglobin H disease. American Journal of Hematology 57:2, pages 160-163.
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A Y Chan, C K So & L C Chan. (1996) Comparison of the HbH inclusion test and a PCR test in routine screening for alpha thalassaemia in Hong Kong.. Journal of Clinical Pathology 49:5, pages 411-413.
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Tsang‐Ming Ko, Li‐Hui Tseng, Fon‐Jou Hsieh & Tzu‐Yao Lee. (2005) Prenatal diagnosis of Hb H disease due to compound heterozygosity for South‐East Asian deletion and Hb constant spring by polymerase chain reaction. Prenatal Diagnosis 13:2, pages 143-146.
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Vivian Chan. (1990) Prenatal diagnosis of alpha and beta thalassemias and hemophilia A: experience in Hong Kong. Clinical Biochemistry 23:1, pages 79-84.
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YujenEdward Hsia, LarryJ. Shapiro, CarolAnne Ford, JohnA. Hunt & NathanS.P. Ching. (1989) MOLECULAR SCREENING FOR HAEMOGLOBIN CONSTANT SPRING. The Lancet 333:8645, pages 988-991.
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