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Hemoglobin
international journal for hemoglobin research
Volume 15, 1991 - Issue 6
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Original Article

Detection of the HB Quong SZE Mutation in a Chinese Family by Selective Amplification of the α2-Globin Gene and Restriction Map Analysis with MSP I

S. Liang Guangxi Medical College Nanning, Guangxi, PR, China
,
X-J. Wen Guangxi Medical College Nanning, Guangxi, PR, China
&
W-X. Lin Guangxi Medical College Nanning, Guangxi, PR, China
Pages 535-540 | Received 01 Mar 1991, Accepted 31 Jul 1991, Published online: 07 Jul 2009

Citations (7)

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Read on this site (3)

Jian-Ying Zhou, Jin-Mei Yan, Jian Li & Dong-Zhi Li. (2016) First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze. Hemoglobin 40:3, pages 210-212.
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Yu Yang, Ji-Wu Lou, Yan-Hui Liu, Yi He & Dong-Zhi Li. (2014) Screening and Diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a Prenatal Control Program for Thalassemia. Hemoglobin 38:3, pages 158-160.
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Hai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, Ru Li, Can Liao & Dong-Zhi Li. (2012) Screening for Common Nondeletional α-Thalassemias in Chinese Newborns by Determination of Hb Bart’s Using the Sebia Capillarys 2 Electrophoresis System. Hemoglobin 36:2, pages 196-199.
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Articles from other publishers (4)

Can Liao, Jian Li, Xing-Mei Xie, Jian-Ying Zhou & Dong-Zhi Li. (2009) Diversity in clinical presentation of hemoglobin H disease induced by the SEA deletion and the hemoglobin Quong Sze. Annals of Hematology 88:11, pages 1145-1147.
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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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R. DARBELLAY, S. MACH‐PASCUAL, K. ROSE, J. GRAF & PH. BERIS. (2008) Haemoglobin Tunis‐Bizerte: a new a globin 129 Leu–> Pro unstable variant with thalassaemic phenotype . British Journal of Haematology 90:1, pages 71-76.
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R. Liang, S. Liang, N. H. Jiang, X‐J. Wen, J‐B. Zhao, J. F. Nechtman, T. A. Stoming & T. H. J. Huisman. (2008) α and β thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization. British Journal of Haematology 86:2, pages 351-354.
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