Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia.
作者信息
Feingold E A, Collins F S, Metherall J E, Stoeckert C J, Weissman S M, Forget B G
出版信息
Ann N Y Acad Sci. 1985;445:159-69. doi: 10.1111/j.1749-6632.1985.tb17185.x.
