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Hemoglobin
international journal for hemoglobin research
Volume 30, 2006 - Issue 3
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ORIGINAL ARTICLE

Prenatal Diagnosis of β-Thalassemia by Reverse Dot-Blot Hybridization in Southern China

Dongzhi Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of ChinaCorrespondence[email protected]
,
Can Liao Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
,
Jian Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
,
Yining Huang Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
,
Xingmei Xie Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
,
Jiaxue Wei Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
&
Shaoqing Wu Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
 show all
Pages 365-370 | Received 27 Oct 2005, Accepted 28 Jan 2006, Published online: 07 Jul 2009

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Zhi-Qing Xiao, Fan Jiang & Dong-Zhi Li. (2023) β-Thalassemia Trait Caused by SUPT5H Defects: Another Case Report. Hemoglobin 47:4, pages 145-146.
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Fan Jiang, Gui-Lan Chen, Jian Li, Xue-Wei Tang & Dong-Zhi Li. (2022) β-Thalassemia Intermedia Caused by the β-Globin Gene 3′ Untranslated Region: Another Case Report. Hemoglobin 46:2, pages 137-139.
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Fan Jiang, Xue-Wei Tang, Jian Li, Jian-Ying Zhou, Lian-Dong Zuo & Dong-Zhi Li. (2021) Hb Lepore-Hong Kong: First Report of a Novel δ/β-Globin Gene Fusion in a Chinese Family. Hemoglobin 45:4, pages 220-224.
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Wen-Juan Wang, Zi-Xuan Ding, Hui-Min Zhang, Ting-Ting Tao, Su-Ning Chen & Ling Xi. (2021) Identification of a Novel β-Thalassemia Mutation at Codon 130 (+T) (HBB: c.391insT) in Han Chinese . Hemoglobin 45:1, pages 46-48.
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Li-Li Xu, Yu Yang, Li Zhen, Min Pan, Jin Han, Jian-Ying Zhou & Dong-Zhi Li. (2020) The Trend in Timing of Prenatal Diagnosis for Thalassemia at a Chinese Tertiary Obstetric Center. Hemoglobin 44:5, pages 325-328.
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Yuan Zhao, Fan Jiang & Dong-Zhi Li. (2020) Hematological Characteristics of β-Globin Gene Mutation –50 (G>A) (HBB: c.-100G>A) Carriers in Mainland China. Hemoglobin 44:4, pages 240-243.
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Jian-Ying Zhou, Fan Jiang, Jian Li, Gui-Lan Chen & Dong-Zhi Li. (2019) Coinheritance of Hb City of Hope (HBB: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization. Hemoglobin 43:2, pages 145-147.
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Gui-Lan Chen, Fan Jiang, Jian Li, Jian-Ying Zhou & Dong-Zhi Li. (2018) Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients. Hemoglobin 42:5-6, pages 306-309.
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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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Yuan Zhao, Lv-Yin Huang, Fan Jiang, Jian-Ying Zhou, Xing-Mei Xie & Dong-Zhi Li. (2017) Hb Hornchurch [β43(CD2)Glu→Lys; HBB: c.130G>A] Compromises the Molecular Diagnosis of β-Thalassemia in a Chinese Family. Hemoglobin 41:4-6, pages 274-277.
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Yan Li, Jin-Mei Yan, Jian-Ying Zhou, Yue-Cheng Lu & Dong-Zhi Li. (2017) Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia. Hemoglobin 41:1, pages 47-49.
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Dong-Zhi Li, Min Pan, Jin Han, Xin Yang, Li Zhen, Jian Li & Yan-Mei Ou. (2016) Prenatal diagnosis of thalassemia in twin pregnancies in mainland China. Journal of Obstetrics and Gynaecology 36:6, pages 731-734.
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Jian Li, Jin-Mei Yan, Xing-Mei Xie, Jian-Ying Zhou, Ru Li & Dong-Zhi Li. (2016) Consequences of Delayed Prenatal Diagnosis of β-Thalassemia in Mainland China. Hemoglobin 40:3, pages 191-193.
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Man-Yu Wu & Dong-Zhi Li. (2016) First Detection of the −27 (A > G) (HBB: c.-77A > G) Mutation of the β-Globin Gene in a Chinese Family. Hemoglobin 40:1, pages 59-60.
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Wenjuan Wang, Qian Wang, Tingting Tao, Aining Sun, Changgeng Ruan & Suning Chen. (2015) Identification of Two Novel β-Thalassemia Mutations (HBB: c.335-346del and HBB: c.108 C > G) in Han Chinese. Hemoglobin 39:5, pages 359-361.
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Man-Yu Wu, Jian Li, Shu-Chen Li, Ru Li, Can Liao & Dong-Zhi Li. (2015) Compound Heterozygosity for HKαα and an in Cis Deletion of Double α Genes Presents as α-Thalassemia Trait. Hemoglobin 39:4, pages 256-259.
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Hua Jiang, Sha Liu, Yong-Ling Zhang, Jun-Hui Wan, Ru Li & Dong-Zhi Li. (2015) Association of an α-Globin Gene Cluster Duplication and Heterozygous β-Thalassemia in a Patient with a Severe Thalassemia Syndrome. Hemoglobin 39:2, pages 102-106.
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Can Liao, Min Pan, Jin Han, Xin Yang, Jian Li, Ru Li & Dong-Zhi Li. (2011) Early Prenatal Diagnosis of Thalassemia: The First Report of Experience in Mainland China. Hemoglobin 35:4, pages 434-438.
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Hailong Huang, Liangpu Xu, Na Lin, Jinbang Xu, Deqin He, Ying Li, Lin Zheng, Hekun Liu & Yuan Lin. (2010) A New β-Thalassemia Deletion Mutation [Codon 36 (–C)] Observed in a Chinese Woman. Hemoglobin 34:6, pages 599-603.
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Ping Yi, Jianxin Guo, Zhuqin Chen, Qiang Liu, Lili Yu, Haichang Xie, Yaohua Yan, Xiaolin Zhong & Li Li. (2010) Misdiagnosis of a β-Thalassemia Heterozygote Using a Reverse Dot-Blot Method may be Caused by a Polymorphic Locus in the Wild Type Sequence of the β-Globin Gene. Hemoglobin 34:2, pages 191-195.
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Can Liao, Xing-Mei Xie, Hui-Zhu Zhong, Jian-Ying Zhou & Dong-Zhi Li. (2009) Proposed Screening Criteria for β-Thalassemia Trait During Early Pregnancy in Southern China. Hemoglobin 33:6, pages 528-533.
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Can Liao, Jian Li & Dongzhi Li. (2008) Association of β-Thalassemia and Hb Q-Thailand Resulting in a Normal Hb A2 Value. Hemoglobin 32:5, pages 505-508.
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Can Liao, Qiong Feng, Jian Li, Yining Huang & Dongzhi Li. (2007) A Double Heterozygote for (δβ)0-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family. Hemoglobin 31:3, pages 397-400.
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Dong‐Zhi Li. (2009) Fetal blood analysis is not a primary method in prenatal diagnosis of thalassemia. European Journal of Haematology 83:1, pages 79-80.
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Dong‐Zhi Li. (2009) Premarital screening for thalassemia in mainland China. Prenatal Diagnosis 29:6, pages 637-638.
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