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Volumn 13, Issue 4, 1989, Pages 325-353

βcluster haplotypes, αgene status, and hematological data from SS, SC, and s-βthalassemia patients in southern California

(7) Schroeder, W A a Powars, Darleen R b Kay, Lois M a Chan, Linda S c Huynh, Van a Shelton, Joan B a Shelton, J Roger a

a CALIFORNIA INSTITUTE OF TECHNOLOGY (United States)

b Division of Hematology Oncology (United States)

c UNIVERSITY OF SOUTHERN CALIFORNIA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN;

ADOLESCENT; ADULT; AGED; CHILD; GENETIC ANALYSIS; GENETIC ENGINEERING; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SICKLE CELL ANEMIA; THALASSEMIA; UNITED STATES;

ADOLESCENT; ADULT; AGED; ANEMIA, SICKLE CELL; CALIFORNIA; CHILD; CHILD, PRESCHOOL; DEOXYRIBONUCLEASE BAMHI; DEOXYRIBONUCLEASE ECORI; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; FETAL HEMOGLOBIN; GLOBINS; HAPLOTYPES; HEMOGLOBIN A2; HEMOGLOBIN SC DISEASE; HUMAN; MIDDLE AGE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; THALASSEMIA;

EID: 0024360719 PISSN: 03630269 EISSN: None Source Type: Journal
DOI: 10.3109/03630268909003397 Document Type: Article

Times cited : (68)

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