Cividalli G G, Antebi S, Klein R, Kerem H, Rachmilewitz E A
Isr J Med Sci. 1976 Nov;12(11):1313-5.
The parents of a child with homozygous thalassemia of the beta O variety requested prenatal diagnosis during a subsequent pregnancy. At the 19th week of pregnancy, a sample of blood containing fetal cells was obtained by placentocentesis. Radiochromatography of globin chains demonstrated production of a beta-chain with a beta/gamma synthetic ratio of 0.049, which is low for this gestational age. The conclusion that the child would be heterozygous for the beta-thalassemia gene was confirmed after birth.
一名患有β⁰型纯合地中海贫血患儿的父母在随后的妊娠期间要求进行产前诊断。在妊娠第19周时,通过胎盘穿刺术获取了一份含有胎儿细胞的血样。珠蛋白链的放射色谱分析显示产生了一条β链,其β/γ合成比为0.049,对于这个孕周来说是低的。出生后证实该胎儿为β地中海贫血基因杂合子。