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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 4
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Original Article

Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. China

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Pages 325-328 | Received 03 Jan 1992, Accepted 06 Mar 1992, Published online: 07 Jul 2009

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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
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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Georgina W. Hall, Swee Lay Thein, Adrian C. Newland, Morag Chisholm, Jan Traeger‐Synodinos, E. Kanavakis, C. Kattamis & Douglas R. Higgs. (2008) A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia. British Journal of Haematology 85:3, pages 546-552.
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