| 引用本文： |
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林伟雄,龙桂芳,李卫,谢建生,金琪,李琪,唐霞.广西地区α地中海贫血高危胎儿产前基因诊断[J].广西科学,1998,5(2):81-82. [点击复制]
- Lin Weixiong,Long Guifang,Li Wei,Xie Jiansheng,Jin Qi,Li Qi,Tang Xia.α-Thalassemia Prenatal Gene Diagnoses in Guangxi Region[J].Guangxi Sciences,1998,5(2):81-82. [点击复制]
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| 摘要: |
| 1989年以来,应用PCR技术选择性扩增α2珠蛋白基因及斑点杂交方法对167例α地中海贫血高危胎儿进行产前基因诊断。结果,HbBart's水肿胎儿27例,HbH病16例,其余为非Bart's水肿胎儿或非HbH病胎儿。 |
| 关键词: α地中海贫血 PCR 产前诊断 |
| DOI： |
| 投稿时间：1998-03-03 |
| 基金项目: |
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| α-Thalassemia Prenatal Gene Diagnoses in Guangxi Region |
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Lin Weixiong, Long Guifang, Li Wei, Xie Jiansheng, Jin Qi, Li Qi, Tang Xia
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| (Laboratory of Hemoglobin, Department of Pediatrics, First Affiliated Hospital, Guangxi Medical University, 6 Binhulu, Nanning, Guangxi, 530021) |
| Abstract: |
| Prenatal gene diagnoses were performed for 167 fetuses who were at the risk of major α-thalassemia since 1989 by using PCR method.As a result,27 fetuses with HbBart's fetal hydrops syndrome and 16 with HbH disease were detected. |
| Key words: α-thalassemia PCR prenatal diagnoses |
