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PMID: 6190397 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Review

Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severity.

American journal of hematology ·Vol. 14 ·No. 4 ·1983-06-00 ·Pages 405-16

Steinberg MH, Hebbel RP

Abstract

暂无摘要

MeSH Terms
Anemia, Sickle Cell/complications,diagnosis,genetics Arterial Occlusive Diseases/etiology Cell Adhesion Chromosome Mapping DNA Restriction Enzymes/analysis Erythrocytes, Abnormal/physiopathology Fetal Hemoglobin/physiology Hemoglobin, Sickle/genetics Hemolysis Humans Splenomegaly/etiology Thalassemia/complications
Chemicals
Hemoglobin, Sickle Fetal Hemoglobin DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Steinberg M H
Hebbel R P
Article Info
Journal
American journal of hematology
Abbr.
Am J Hematol
ISSN
0361-8609
DOI
10.1002/ajh.2830140412
Published
1983-06-00
Pages
405-16
Language
English
Region
United States
NLM ID
7610369
Subset
IM
Grants
NHLBI NIH HHS · HB73005 · United States
NHLBI NIH HHS · HL26139 · United States
External Links
PubMed source DOI: 10.1002/ajh.2830140412 View journal details
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