Outcome in hemoglobin SC disease: A four-decade observational study of clinical, hematologic, and genetic factors

American Journal of Hematology

Volumn 70, Issue 3, 2002, Pages 206-215

  Powars, Darleen R ^a   Hiti, Alan ^a   Ramicone, Emily ^a   Johnson, Cage ^a   Chan, Linda ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

Hemoglobin SC; Outcome

Indexed keywords

HEMOGLOBIN F;

ADULT; ALPHA THALASSEMIA; ARTICLE; AVASCULAR NECROSIS; CLINICAL OBSERVATION; FEMALE; GENETIC ANALYSIS; HAPLOTYPE; HEMATOLOGY; HEMOGLOBIN SC DISEASE; HEMOGLOBINOPATHY; HUMAN; MAJOR CLINICAL STUDY; MALE; OUTCOMES RESEARCH; PRIORITY JOURNAL; REHYDRATION; TISSUE SPECIFICITY;

ADOLESCENT; ADULT; ALPHA-THALASSEMIA; CHILD; CHILD, PRESCHOOL; ERYTHROCYTE INDICES; EYE DISEASES; FETAL HEMOGLOBIN; GLOBINS; HAPLOTYPES; HEMOGLOBIN SC DISEASE; HEMOGLOBINS; HUMANS; INFANT; INFANT, NEWBORN; MIDDLE AGED; MORBIDITY; OSTEONECROSIS; POLYMERASE CHAIN REACTION;

EID: 0036085773     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajh.10140     Document Type: Article

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