Complex interactions of δβ hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (β26 g→a) and α+ thalassaemia in a Thai family

European Journal of Haematology

Volumn 68, Issue 2, 2002, Pages 107-111

  Viprakasit, Vip ^c   Pung Amritt, Parichat ^a   Suwanthon, Lerlugh ^a   Clark, Kevin ^b   Tanphaichitr, Voravarn S ^a  

^a MAHIDOL UNIVERSITY   (Thailand)

^b JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^c NONE

Author keywords

+ thalassaemia; Haemoglobin E; Haemoglobin Lepore Hollandia

Indexed keywords

ADOLESCENT; ALPHA THALASSEMIA; ARTICLE; BETA THALASSEMIA; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; GENE INTERACTION; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HEMATOLOGIC DISEASE; HEMOGLOBIN LEPORE HOLLANDIA; HEMOGLOBINOPATHY; HUMAN; HYBRID; MALE; MOLECULAR DYNAMICS; PRIORITY JOURNAL; SCHOOL CHILD; THAILAND; CHILD; FAMILY HEALTH; GENE DELETION; GENETICS; HEMOGLOBIN LEPORE; NUCLEOTIDE SEQUENCE;

GLOBIN; HEMOGLOBIN E; HEMOGLOBIN VARIANT;

ADOLESCENT; ALPHA-THALASSEMIA; CHILD; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; GLOBINS; HEMOGLOBIN E; HEMOGLOBINOPATHIES; HEMOGLOBINS, ABNORMAL; HUMANS; MALE; SEQUENCE DELETION; THAILAND; VARIATION (GENETICS);

EID: 0035983105     PISSN: 09024441     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0609.2002.01637.x     Document Type: Article

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