Compound heterozygote state for Gγ Aγ(δβ)°-thalassemia and hereditary persistence of fetal hemoglobin

American Journal of Hematology

Volumn 80, Issue 2, 2005, Pages 119-123

  Fucharoen, Supan ^a   Panyasai, Sitthichai ^a   Surapot, Satja ^b   Fucharoen, Goonnapa ^a   Sanchaisuriya, Kanokwan ^a  

^a KHON KAEN UNIVERSITY   (Thailand)

^b Maharat Nakhon Si Thammarat Hospital   (Thailand)

Author keywords

thalassemia; HPFH 6; Thalassemia intermedia

Indexed keywords

GAMMA GLOBIN; GLOBIN; HEMOGLOBIN F;

ADULT; ARTICLE; BETA THALASSEMIA; CASE REPORT; CHROMOSOME INVERSION; GAMMA ALPHA DELTA BETA THALASSEMIA; GENE DELETION; GENE INTERACTION; HEMATOCRIT; HEMOGLOBIN ANALYSIS; HEMOGLOBIN DETERMINATION; HETEROZYGOSITY; HUMAN; MALE; MEAN CORPUSCULAR HEMOGLOBIN; MEAN CORPUSCULAR VOLUME; PRIORITY JOURNAL; THAILAND; THALASSEMIA;

ADULT; BETA-THALASSEMIA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FETAL HEMOGLOBIN; HEMOGLOBINS; HETEROZYGOTE; HUMANS; INHERITANCE PATTERNS; MALE; SEQUENCE DELETION; THAILAND;

EID: 26444555585     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajh.20426     Document Type: Article

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