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

The Types and Distribution of α-Thalassemia-2 in China

Y. T. Zeng Laboratory of Medical Genetics, Shanghai Children's Hospital Shanghai, P.R., China
,
S. Z. Huang Laboratory of Medical Genetics, Shanghai Children's Hospital Shanghai, P.R., China
&
H. J. Chen Laboratory of Medical Genetics, Shanghai Children's Hospital Shanghai, P.R., China
Pages 455-458 | Received 05 Jan 1988, Accepted 01 Jun 1988, Published online: 07 Jul 2009

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Jing-Zhong Liu, Mei Yan, Li-Rong Wang, Zhan-Yong Wang, Yin-Ping Fan, Bai Xiao & Yan Zhou. (2008) Molecular Prenatal Diagnosis of α-Thalassemia Using Real-Time and Multiplex Polymerase Chain Reaction Methods. Hemoglobin 32:6, pages 553-560.
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Ren Cai, Jingzhong Liu, Lirong Wang, Xin Liang, Bai Xiao, Liu Su, Yan Zhou & Lizhen Pan. (2004) Study on Molecular Epidemiology of the α‐Thalassemias in Liuzhou City, Guangxi Autonomous Region, China . Hemoglobin 28:4, pages 325-333.
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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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Xiaofeng GU & Yitao Zeng. (2002) A Review of the Molecular Diagnosis of Thalassemia. Hematology 7:4, pages 203-209.
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M. L. Ribeiro & G. P. Tamagnini. (1997) Hemoglobin Disorders in Macao. Hemoglobin 21:3, pages 271-279.
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X-J. Wen, S. Liang, Q. Jin & W-X. Lin. (1992) The Nondeletional Types of HB H Disease in Guangxi. Hemoglobin 16:1-2, pages 45-50.
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Jing-Bo Zhao, Lin Zhao, Y-C. Gu & T. H. J. Huisman. (1992) Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. China. Hemoglobin 16:4, pages 325-328.
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S. Liang, X-J. Wen & W-X. Lin. (1991) 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. Hemoglobin 15:6, pages 535-540.
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Y. Hattori, M. Morishita, Y. Yamashiro, Ki. Yamamoto, Ku. Yamamoto, Y. Matsuno, Y. Ohba & T. Miyaji. (1990) Three Japanese Families with Hb H Disease: Gene Anals and Their Characterizations. Hemoglobin 14:5, pages 559-567.
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Articles from other publishers (4)

Henu Kumar Verma, Saikrishna Lakkakula & Bhaskar V.K.S. Lakkakula. (2018) Retrospection of the effect of hydroxyurea treatment in patients with sickle cell disease. Acta Haematologica Polonica 49:1, pages 1-8.
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Jingzhi ZhangJingbin YanFanyi Zeng. (2018) Recent Progress on Genetic Diagnosis and Therapy for β-Thalassemia in China and Around the World. Human Gene Therapy 29:2, pages 197-203.
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Yi-tao Zeng & Shu-zhen Huang. (2001) The studies of hemoglobinopathies and thalassemia in China—the experiences in Shanghai Institute of Medical Genetics. Clinica Chimica Acta 313:1-2, pages 107-111.
Crossref
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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