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本文报道对3例蚕豆病患者的家庭成员245人作了患病史调查,井用高铁血红蛋白还原试验对169人作了红细胞G6PD缺陷的调查,再次证明此种缺陷是按伴性不完全显性规律遗传的。
In this paper, 245 cases of familial members of 3 Vicia faba patients were investigated for their medical history. We investigated the G6PD deficiency of 169 human erythrocytes by methemoglobin reduction test, and again proved that this kind of defect was based on the incomplete dominance Regular genetic.