Abstract
A newly developed HPLC procedure (1) was used to study the percentages of Gγ and Aγ chains in the Hb F from newborn and patients with sickle cell anemia. The method gives data comparable to those obtained with a more laborious chemical procedure. However, the presence of the AγT chain, i.e., the Aγ chain with an Ile→Thr substitution at position 75, interferes with the determination of the Gγ to Aγ ratio because the aγt and Gγ chains have the same chromatographic mobility.