Screening for (--SEA) alpha-globin gene deletion in beta-thalassemia carriers and prevention of hydrops fetalis | Haematologica

ES Kwan Ma; AY Yin Chan; S Yin Ha; GC Fung Chan; Y Lung Lau; LC Chan

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Screening for (--SEA) alpha-globin gene deletion in beta-thalassemia carriers and prevention of hydrops fetalis | Haematologica

机译：β地中海贫血携带者中（-SEA）α-珠蛋白基因缺失的筛选和胎儿积水的预防血液学

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来源
《Haematologica》 |2000年第9期|共3页
作者
ES Kwan Ma; AY Yin Chan; S Yin Ha; GC Fung Chan; Y Lung Lau; LC Chan;
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中图分类血液及淋巴系疾病;
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1. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening | Haematologica [J] . D Li, C Liao, J Li, Haematologica . 2006,第5期

机译：通过产前筛查检测β-地中海贫血携带者中的α-地中海贫血并预防胎儿Hb Bart胎儿水肿|血液学
2. Analysis of real-time SYBR-polymerase chain reaction cycle threshold for diagnosis of the alpha-thalassemia-1 Southeast Asian type deletion: application to carrier screening and prenatal diagnosis of Hb Bart's hydrops fetalis. [J] . Pornprasert S, Sukunthamala K, Sacome J, Hemoglobin: International Journal for Hemoglobin Research . 2008,第4期

机译：实时SYBR聚合酶链反应周期阈值分析，用于诊断α-地中海贫血1东南亚型缺失：在Hb Bart胎儿积水的携带者筛查和产前诊断中的应用。
3. Interaction between (--SEA) alpha-thalassemia deletion and uncommon non-deletional alpha-globin gene mutations in Chinese patients | Haematologica [J] . ES Ma, EY Chow, AY Chan, Haematologica . 2001,第5期

机译：中国患者中（--SEA）α-地中海贫血缺失与罕见的非缺失性α-珠蛋白基因突变之间的相互作用血液学
4. FISH for Carrier Detection of large Deletions in the Factor VIII Gene [C] . T. Forster, M. Guttenbach, C.R. Muller, Hemophilie-Symposion . 2004

机译：FISH用于载体检测因子VIII基因的大缺失
5. Correction of mouse models of sickle cell disease and beta-thalassemia using stem cell and genetic-based therapy. [D] . Levasseur, Dana N. 2003

机译：使用干细胞和基于基因的疗法校正镰状细胞病和β地中海贫血的小鼠模型。
6. Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart’s hydrops fetalis syndrome [O] . Wittaya Jomoui, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, -1

机译：东南亚人群α0地中海贫血（SEA缺失）的遗传起源及其在Hb Bart胎儿水肿胎儿综合征的准确产前诊断中的应用
7. Severe perinatal hydrops fetalis in genome edited pigs with a biallelic five base pair deletion of the Marfan syndrome gene, FBN1 [O] . Hiu-Gwen Tsang, Simon Lillico, Christopher Proudfoot, 2020

机译：严重的围产期水产胎儿在基因组编辑猪中，具有双倍曲率的五个碱基对缺失Marfan综合征基因，FBN1

Screening for (--SEA) alpha-globin gene deletion in beta-thalassemia carriers and prevention of hydrops fetalis | Haematologica

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