Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.
作者信息
Fensom A H, Benson P F, Rodeck C H, Campbell S, Gould J D
出版信息
Br Med J. 1979 Jan 6;1(6155):21-2. doi: 10.1136/bmj.1.6155.21-a.
Abstract
摘要
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Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.通过胎儿血液酶测定对半乳糖血症杂合子进行产前诊断。
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Value of fetoscopy in prenatal diagnosis.胎儿镜检查在产前诊断中的价值。
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本文引用的文献
1
Prenatal diagnosis of galactosaemia.半乳糖血症的产前诊断。
Br Med J. 1974 Nov 16;4(5941):386-7. doi: 10.1136/bmj.4.5941.386.
2
Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemia.用于半乳糖血症产前诊断的培养羊膜细胞中1-磷酸半乳糖尿苷转移酶的测定
Clin Chim Acta. 1975 Jul 23;62(2):189-94. doi: 10.1016/0009-8981(75)90227-2.
3
Sampling pure fetal blood by fetoscopy in second trimester of pregnancy.在妊娠中期通过胎儿镜采集纯净胎儿血液。
Br Med J. 1978 Sep 9;2(6139):728-30. doi: 10.1136/bmj.2.6139.728.
4
Early prenatal diagnosis of neural-tube defects by ultrasound-guided fetoscopy.
Lancet. 1978 May 27;1(8074):1128-9. doi: 10.1016/s0140-6736(78)90303-3.
5
Prenatal diagnosis in Duchenne muscular dystrophy: Salvage of normal male fetus.杜氏肌营养不良症的产前诊断：挽救正常男性胎儿。
Lancet. 1978 Jan 14;1(8055):90. doi: 10.1016/s0140-6736(78)90021-1.
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