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AB128. The first report of a hereditary persistent fetal hemoglobinemia of the Southeast Asian type deletion in the North of Vietnam

机译：AB128。越南北部东南亚型遗传性遗传性遗传性胎儿血红蛋白血症的首次报道

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BackgroundBeta thalassemia is one of the most common single gene disorders worldwide and also in Vietnam. In this study, we reported, for the first time, a hereditary persistent fetal hemoglobinemia (HPFH) of the Southeast Asian (SEA) type deletion in the North of Vietnam.

机译：背景β地中海贫血是世界范围内以及越南最常见的单基因疾病之一。在这项研究中，我们首次报道了越南北部东南亚（SEA）型遗传性持续性胎儿血红蛋白血症（HPFH）。

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期刊名称 Annals of Translational Medicine
作者
Ly Thi Thanh Ha;
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年(卷),期 2017(5),Suppl 2
年度 2017
页码 AB128
总页数 1
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1. Analysis of real-time PCR cycle threshold of alpha-thalassemia-1 Southeast Asian type deletion using fetal cell-free DNA in maternal plasma for noninvasive prenatal diagnosis of Bart's hydrops fetalis. [J] . Pornprasert S, Sukunthamala K, Kunyanone N, Journal of the Medical Association of Thailand =: Chotmaihet thangphaet . 2010,第11期

机译：使用母体血浆中的胎儿无细胞DNA实时分析α-地中海贫血1东南亚型缺失的实时PCR循环阈值，以进行无创性Bart胎儿积水的产前诊断。
2. Analysis of real-time PCR cycle threshold of alpha-thalassemia-1 Southeast Asian type deletion using fetal cell-free DNA in maternal plasma for noninvasive prenatal diagnosis of Bart's hydrops fetalis. [J] . Pornprasert S, Sukunthamala K, Kunyanone N, Journal of the Medical Association of Thailand =: Chotmaihet thangphaet . 2010,第11期

机译：使用母体血浆中的胎儿无细胞DNA实时分析α-地中海贫血1东南亚型缺失的实时PCR循环阈值，以进行无创性Bart胎儿积水的产前诊断。
3. Detection of α-thalassemia-1 Southeast Asian and Thai Type Deletions and β-thalassemia 3.5-kb Deletion by Single-tube Multiplex Real-time PCR with SYBR Green1 and High-resolution Melting Analysis [J] . Annals of laboratory medicine. . 2011,第3期

机译：SYBR Green1单管多重实时PCR和高分辨率熔解分析法检测α-地中海贫血-1东南亚和泰国型缺失和β-地中海贫血3.5-kb缺失
4. Research on the Industrial Strategic Transfer of Vietnam and Other Southeast Asian Countries under the Background of “Intemet+” [C] . Jiayu Lai Dahe Fortune China Forum and Chinese High-educational Management Annual Academic Conference . 2020

机译：越南和其他东南亚国家在“intemet +”背景下的产业战略转移研究
5. JAPAN'S SOUTHEAST ASIAN POLICY IN THE POST-VIETNAM ERA (1975-1985). [D] . KHAMCHOO, CHAIWAT. 1986

机译：越南后时代的日本东南亚政策（1975-1985年）。
6. Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5′δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia [O] . Elyes Slim Ghedira, Serge Pissard 2013

机译：携带Thai（δβ）0缺失和土耳其语（δβ）0缺失/倒置的患者的胎儿血红蛋白率低强化了以下假设：5δBCL11A结合位点在其胎儿血红蛋白抑制调节中起主要作用。对β-珠蛋白基因簇中12.6 kb的缺失是东南亚常见的已知泰国/越南（δβ）0地中海贫血的回应
7. Detection of α-thalassemia-1 Southeast Asian and Thai Type Deletions and β-thalassemia 3.5-kb Deletion by Single-tube Multiplex Real-time PCR with SYBR Green1 and High-resolution Melting Analysis [O] . Pornprasert, Sakorn, Wiengkum, Thanatcha, Srithep, Sarinee, 2011

机译：SYBR Green1单管多重实时PCR和高分辨率熔解分析法检测α-地中海贫血-1东南亚和泰国型缺失和β-地中海贫血3.5-kb缺失
8. Psychological Operations Against North Vietnam, July 1972-January 1973 (Project CHECO Southeast Asia Report) [R] . Tinius, J. L. 1974

机译：1972年7月至1973年1月对北越的心理行动（CHECO东南亚项目报告）

AB128. The first report of a hereditary persistent fetal hemoglobinemia of the Southeast Asian type deletion in the North of Vietnam

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