Hemoglobin S/O(ARAB): Thirteen new cases and review of the literature

American Journal of Hematology

Volumn 60, Issue 4, 1999, Pages 279-284

  Zimmerman, Sherri A ^a   O'Branski, Erin E ^a   Rosse, Wendell F ^a   Ware, Russell E ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Hemoglobin O(Arab); Hemoglobin S; Sickle cell disease

Indexed keywords

BETA GLOBIN; CELLULOSE ACETATE; CITRIC ACID;

ADOLESCENT; ADULT; ARTICLE; CARDIOVASCULAR DISEASE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; ELECTROPHORESIS; FEMALE; HEMOGLOBINOPATHY; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; OSTEOMYELITIS; PH MEASUREMENT; PRIORITY JOURNAL; RETICULOCYTE COUNT; SICKLE CELL ANEMIA;

ADOLESCENT; ADULT; AFRICAN CONTINENTAL ANCESTRY GROUP; ANEMIA, HEMOLYTIC; CHILD; CHILD, PRESCHOOL; ELECTROPHORESIS, CELLULOSE ACETATE; ERYTHROCYTE INDICES; ERYTHROCYTES; FEMALE; GLOBINS; HEMOGLOBIN, SICKLE; HEMOGLOBINOPATHIES; HEMOGLOBINS, ABNORMAL; HETEROZYGOTE; HUMANS; HYPERBILIRUBINEMIA; MALE; MIDDLE AGED; MUTATION; RETICULOCYTE COUNT;

EID: 0032903492     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199904)60:4<279::AID-AJH5>3.0.CO;2-2     Document Type: Article

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