Molecular studies of haemoglobin-E in tribal populations of Tripura [6]

Lancet

Volumn 349, Issue 9061, 1997, Pages 1297-

  De, Madhusnata ^a   Chakraborty, Gouri ^b   Das, Swapan Kr ^b   Bhattacharya, D K ^b   Talukder, Geeta ^b  

^a VIVEKANANDA INSTITUTE OF MEDICAL SCIENCES   (India)

^b Victoria Memorial Hospital   (India)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; HEMOGLOBIN E;

BETA THALASSEMIA; BLOOD SAMPLING; ETHNIC GROUP; HEMOGLOBIN DETERMINATION; HOMOZYGOTE; HUMAN; INDIA; LETTER; NORMAL HUMAN; POINT MUTATION; POPULATION GENETICS; PRIORITY JOURNAL;

EID: 0343035713     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(05)62509-3     Document Type: Article

References (5)

1. Winichagoon P, Thonglairoam V, Fucharoen S, Wilairat P, Fukumaki Y, Wasi P. Severity differences in β-thalassaemia/ haemoglobin E syndromes; implication of genetic factor. Br J Haematol 1993; 83: 633-39.
2. Weatherall DJ, Clegg JB. Thalassemia-a global public health problem. N at Med 1996; 2: 847-49.
3. Ajmani M, Sharma A, Talukder G, Bhattacharya DK. Haemoglobin variants in India. Acta Genet Med Gemellol 1979; 27: 11-30.
4. Old JM, Varawalla NY, Weatherall DJ. The rapid detection and prenatal diagnosis of β-thalassaemia in the Asian Indian and Cypriot populations in the UK. Lancet 1990; 336: 834-37.
5. E globin gene. Nature 1982; 300: 768-69.