..., quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. α-thalassemia Caucasian population Hemoglobin S Saudi Arabs Acta haemat. 45...

...George R. Honig; George Mason; Loyda N. Vida Folic acid deficiency has been reported to produce a substantial change in the ratio of hemoglobin S to hemoglobin A in the blood of individuals having sickle cell trait. Synthesis of the specific β -chains of these hemoglobins was studied before...

...Cyril Levene; Eliezer A. Rachmilewitz; Eric Ezekiel; Emil Freundlich; Gerald Sandler Blood group phenotypes of anthropologic significance are described for inhabitants of two Israeli Arab communities with foci of hemoglobin S (HbS). The presence of Fy(a-b-), Rh₀, hr V+ , and Js(a+) among the Hulah...

...Eugene F. Roth; Eliezer H. Rachmilewitz; Alicia Schifter; Ronald L. Nagel Arabs living near the Sea of Galilee were found to be homozygous for hemoglobin S. Studies of solubility, mechanical precipitability, electrophoretic mobility on starch-gel and citrate agar media, minimum gelling...

...Gerald Sandler; Gino Schilirò; Antonio Russo; Salvatore Musumeci; Eliezer A. Rachmilewitz As an approach to investigating the origin of sickle cell hemoglobin (hemoglobin S) in white persons of Sicilian ancestry, two groups of native Sicilians were tested for blood group evidence of African...