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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 3
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Short Communication

A Double Heterozygote for (δβ)0-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family

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Pages 397-400 | Received 10 Nov 2006, Accepted 26 Dec 2006, Published online: 07 Jul 2009

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Fan Jiang, Gui-Lan Chen, Jian Li, Jian-Ying Zhou, Can Liao & Dong-Zhi Li. (2018) Analysis of the Genotypes in a Chinese Population with Increased Hb A2 and Low Hematological Indices. Hemoglobin 42:3, pages 154-158.
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Fan Jiang, Liandong Zuo, Dongzhi Li, Jian Li, Xuewei Tang, Guilan Chen, Jianying Zhou, Hang Lu & Can Liao. (2020) Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China. BMC Medical Genetics 21:1.
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Afshan Sumera, Nur Diana Anuar, Ammu Kutty Radhakrishnan, Hishamshah Ibrahim, Nurul H. Rutt, Nur Hafiza Ismail, Ti-Myen Tan & Abdul Aziz Baba. (2020) A Novel Method to Identify Autoantibodies against Putative Target Proteins in Serum from beta-Thalassemia Major: A Pilot Study. Biomedicines 8:5, pages 97.
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W.‐J. Cai, J. Li, X.‐M. Xie & D.‐Z. Li. (2015) Screening for common β‐globin gene cluster deletions in Chinese individuals with increased hemoglobin F. International Journal of Laboratory Hematology 37:6, pages 752-757.
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