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Volumn 25, Issue 1, 2001, Pages 91-96

Thalassemia intermedia and extramedullary hematopoiesis associated with compound heterozygosity for the 532 bp deletion of the β-globin gene and gene deletion hereditary persistence of fetal hemoglobin

(3) Qu, G a Elkins, S a Steinberg, M H a

a BOSTON UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN F;

ADULT; ARTICLE; BASE PAIRING; CASE REPORT; ERYTHROPOIESIS; EXTRAMEDULLARY HEMATOPOIESIS; GENE DELETION; GENE MUTATION; GENETIC DISORDER; HEMATOPOIESIS; HETEROZYGOSITY; HUMAN; MALE; MICROCYTOSIS; PHENOTYPE; SPLENOMEGALY; THALASSEMIA;

ADULT; AFRICAN CONTINENTAL ANCESTRY GROUP; BETA-THALASSEMIA; CODON; DNA MUTATIONAL ANALYSIS; FEMALE; FETAL HEMOGLOBIN; GENE FREQUENCY; GLOBINS; HEMATOPOIESIS, EXTRAMEDULLARY; HEMOGLOBINOPATHIES; HETEROZYGOTE; HUMANS; MALE; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; SEQUENCE DELETION; SPLENOMEGALY;

EID: 0035094433 PISSN: 03630269 EISSN: None Source Type: Journal
DOI: 10.1081/HEM-100103073 Document Type: Article

Times cited : (1)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.