Monozygotic Twins with Sickle Cell Anemia and Discordant Clinical Courses: Clinical and Laboratory Studies-Reference-Cited by-同舟云学术

Monozygotic Twins with Sickle Cell Anemia and Discordant Clinical Courses: Clinical and Laboratory Studies

Published:1991-01 Issue:4 Volume:15 Page:247-256
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Amin R. R.,Bauersachs R. M.,Meiszlman H. J.,Hlohandas N.,Hebbel R. P.,Bowen P. E.,Schlegel R. A.,Williamson P.,Westerman M. P.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269109027877

Reference27 articles.

1. Editorial: Delay time of gelation: a possible determinant of clinical severity in sickle cell disease

2. Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?

3. Dover G. J., Charache S. Progress in Clinical and Biological Research, Pathophysiological Aspects of Sickle Cell Vaso-Occlusion, R. L. Nagel. Alan R. Liss, Inc., New York 1987; Vol. 240: 277

4. Hematologically and Genetically Distinct Forms of Sickle Cell Anemia in Africa

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