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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 1
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Original Article

Direct Demonstration of the hb Suan-Dok Mutation in the Q2-Globin Gene by Restriction Analysis with Sma I

J. Hundrieser Department of Human Genetics, Medizinische Hochschule Hannover, D-3000, Hannover 61, Federal Republic of Germany
,
T. Sanguansermsri Human Genetics Unit, Faculty of Medicine Chiangmai University, Chiangmai, Thailand
,
M. Laig Department of Human Genetics, Medizinische Hochschule Hannover, D-3000, Hannover 61, Federal Republic of Germany
,
M. Pape Department of Human Genetics, Medizinische Hochschule Hannover, D-3000, Hannover 61, Federal Republic of Germany
,
W. Kiihnau Department of Human Genetics, Medizinische Hochschule Hannover, D-3000, Hannover 61, Federal Republic of Germany
&
G. Flatz Department of Human Genetics, Medizinische Hochschule Hannover, D-3000, Hannover 61, Federal Republic of Germany; Human Genetics Unit, Faculty of Medicine Chiangmai University, Chiangmai, Thailand
Pages 69-77 | Received 05 May 1989, Accepted 11 Jan 1990, Published online: 07 Jul 2009

Citations (6)

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Marlies E. Regtuijt, Cornelis L. Harteveld, Peter Van Delft, Nicole Akkermans & Piero C. Giordano. (2004) Hb Suan‐Dok [α109(G16)Leu→Arg; CTG→CGG (α2)] Described in a Patient of African Ancestry. Hemoglobin 28:3, pages 173-176.
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T. H.J. Huisman & M. F.H. Carver. (1998) The Thalassemia Repository (Ninth Edition; Part II). Hemoglobin 22:3, pages 287-310.
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Articles from other publishers (4)

Thanyachai Sura, Objoon Trachoo, Vip Viprakasit, Prin Vathesatogkit, Atchara Tunteeratum, Manisa Busabaratana, Raewadee Wisedpanichkij & Parttraporn Isarangkura. (2007) Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method. Annals of Hematology 86:9, pages 659-663.
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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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Antonios C. Kattamis, Clara Camaschella, Piera Sivera, Saul Surrey & Paolo Fortina. (1998) Human α‐Thalassemia syndromes: Detection of molecular defects . American Journal of Hematology 53:2, pages 81-91.
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T. P. Molchanova, D. D. Pobedimskaya & T. H. J. Huisman. (1994) The differences in quantities of α2-and α1-globin gene variants in heterozygotes. British Journal of Haematology 88:2, pages 300-306.
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