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This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Rights and Permissions Citing Articles Citing Articles via CrossRef Citing Articles via Google Scholar Google Scholar Articles by WOLFF, J. A. Articles by VON HOFE, F. H. Search for Related Content PubMed PubMed Citation Articles by WOLFF, J. A. Articles by VON HOFE, F. H. Social Bookmarking                   What's this?  Previous Article  |  Table of Contents  |  Next Article  Blood, 1958, Vol. 13, No. 5, pp. 492-501. © 1958 American Society of Hematology, Inc. Hemoglobin H-Thalassemia Disease JAMES A. WOLFF 1, RICHARD H. MICHAELS 1, and FREDERICK H. VON HOFE 1 1 Department of Pediatrics, Columbia University, and the Babies Hospital New York City, N. Y. A child of Italian parentage is presented as an example of Hgb H-thalassemia disease. A family study is included. Previous documented reports have included individuals of Chinese, Thai, Greek and Filipino parentage. Genetic aspects of the association of Hgb H with thalassemia are discussed. It is suggested that the study of other patients who present a clinical picture resembling mild Cooley’s anemia may reveal the presence of hemoglobin variants. Submitted on September 14, 1957 Accepted on November 25, 1957 CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    What's this?

	Copyright © 1958 by American Society of Hematology         Online ISSN: 1528-0020