Marengo-Rowe A J, McCracken A W, Flanagan P
J Clin Pathol. 1968 Jul;21(4):508-10. doi: 10.1136/jcp.21.4.508.
A family study is reported in which all three siblings were shown to be doubly heterozygous for haemoglobin D Los Angeles and beta thalassaemia, which resulted in a complete suppression of haemoglobin A synthesis. This demonstrates the effects of genetic interaction which occur when the genes for haemoglobin D Los Angeles and beta thalassaemia are both transmitted to the offspring. The importance of family studies in the investigation of haemoglobin abnormalities is stressed.
本文报道了一项家系研究,该家系的所有三个兄弟姐妹均被证明为血红蛋白D洛杉矶和β地中海贫血的双重杂合子,这导致血红蛋白A合成完全受到抑制。这证明了当血红蛋白D洛杉矶和β地中海贫血的基因都传递给后代时发生的基因相互作用的影响。强调了家系研究在血红蛋白异常调查中的重要性。