Kendall A, Pang W
Hum Hered. 1980;30(1):50-3. doi: 10.1159/000153089.
A Chinese family is described in which 6 members possess both the beta-chain hemoglobin variant Hb New York and alpha-thalassemia trait. The frequency of this combination may be greater than hitherto realized because Hb New York may easily be missed on routine hemoglobin electrophoresis.
本文描述了一个中国家庭,其中6名成员同时拥有β链血红蛋白变体Hb纽约和α地中海贫血特征。这种组合的频率可能比迄今所认识到的更高,因为在常规血红蛋白电泳中Hb纽约可能很容易被漏检。