Hemoglobin New York Associated with Alpha-Thalassemia

Abstract
A Chinese family is described in which 6 members possess both the β-chain hemoglobin variant Hb New York and α -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.

This publication has 1 reference indexed in Scilit: