用于甲型血友病产前诊断的凝血因子 VIII 基因特异性探针。 - Suppr | 超能文献

Factor VIII gene specific probe for prenatal diagnosis of haemophilia A.

作者信息

Din N, Schwartz M, Kruse T, Vestergaard S R, Ahrens P, Caput D, Hartog K, Quiroga M

出版信息

Lancet. 1985 Jun 22;1(8443):1446-7. doi: 10.1016/s0140-6736(85)91873-2.

DOI:10.1016/s0140-6736(85)91873-2

Abstract

摘要

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Factor VIII gene specific probe for prenatal diagnosis of haemophilia A.用于甲型血友病产前诊断的凝血因子 VIII 基因特异性探针。

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Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements.通过因子VIII活性和抗原检测对一个甲型血友病家庭进行产前诊断。

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Carrier detection and prenatal diagnosis in haemophilia A and B.甲型和乙型血友病的携带者检测与产前诊断。

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Antenatal diagnosis and carrier detection of haemophilia A using factor VIII gene probe.应用因子VIII基因探针进行甲型血友病的产前诊断及携带者检测。

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Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.作为甲型血友病分子诊断标志物的凝血因子VIII基因部分缺失

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Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.凝血因子VIII基因倒位：荷兰甲型血友病家庭携带者检测及产前诊断的改进

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[Prenatal diagnosis for fetus with hemophilia A].[甲型血友病胎儿的产前诊断]

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Diagnosis of genetic disease using recombinant DNA.使用重组DNA诊断遗传疾病。

Hum Genet. 1986 May;73(1):1-11. doi: 10.1007/BF00292654.

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A new HindIII restriction fragment length polymorphism in the hemophilia A locus.甲型血友病基因座中一种新的HindIII限制性片段长度多态性。

Hum Genet. 1987 Jun;76(2):127-8. doi: 10.1007/BF00284907.

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De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosis.

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