Prenatal diagnosis of β-thalassemia major by high-performance liquid chromatography analysis of hemoglobins in fetal blood samples

Hemoglobin

Volumn 25, Issue 1, 2001, Pages 19-27

  Sanguansermsri, T ^a   Thanarattanakorn, P ^a   Steger, H F ^a   Tongsong, T ^a   Chanprapaph, P ^a   Wanpirak, C ^a   Siriwatanapa, P ^a   Sirichotiyakul, S ^a   Flatz, G ^a  

^a Faculty of Medicine Chiang Mai University   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN; HEMOGLOBIN A; HEMOGLOBIN A2;

ARTICLE; CLINICAL ARTICLE; CORDOCENTESIS; ERYTHROCYTE FRAGILITY; FETUS; GENE MUTATION; GENE SEQUENCE; HETEROZYGOSITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIGH RISK PATIENT; HOMOZYGOSITY; HUMAN; PRENATAL DIAGNOSIS; THAILAND; THALASSEMIA MAJOR;

ADULT; BETA-THALASSEMIA; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CODON; CODON, NONSENSE; CORDOCENTESIS; DNA MUTATIONAL ANALYSIS; FEMALE; FETAL BLOOD; FETAL DISEASES; GENOTYPE; GESTATIONAL AGE; GLOBINS; HEMOGLOBINS, ABNORMAL; HUMANS; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; PROMOTER REGIONS (GENETICS); PROSPECTIVE STUDIES; SEQUENCE DELETION; SPECIMEN HANDLING; THAILAND;

EID: 0035088922     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-100103066     Document Type: Article

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