Red cell genetic abnormalities, β-globin gene haplotypes, and APOB polymorphism in the Great Andamanese, a primitive Negrito tribe of Andaman and Nicobar Islands, India

Human Biology

Volumn 73, Issue 5, 2001, Pages 739-744

  Murhekar, K M ^a   Murhekar, M V ^a   Mukherjee, M B ^a   Gorakshakar, A C ^a   Surve, R ^a   Wadia, M ^a   Phanasgaonkar, S ^a   Shridevi, S ^a   Colah Roshan, B ^a   Mohanty, D ^a  

^a Regl Medical Research Centre ICMR   (India)

Author keywords

Andaman; Apolipoprotein B; G6PD deficiency; Hemoglobinopathies

Indexed keywords

EID: 0035201107     PISSN: 00187143     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)

1. E globin gene in Southeast Asia
2. DPIP decolourisation test for G6PD deficiency
3. Application of co-valent reverse dot blot hybridization for rapid prenatal diagnosis of the common Indian thalassemia syndromes
4. Rapid detection of hypervariable regions by the polymerase chain reaction technique
5. Population dynamics of haemoglobinopathes in S. E. Asia
6. β-globin gene linked DNA haplotypes and frameworks in three Southeast Asia populations
7. A new Glucose-6-Phosphate Dehydrogenase variant, G6PD Orissa (44 Ala(Gly), is the major polymorphic variant in tribal populations in India
8. E globin gene
9. S mutation and the unicentric origin of the tribal populations of India
10. The effect of β-thalassemia on sickle cell anemia linked to the Arab-Indian haplotype among a tribal and non-tribal population in India
11. Linkage of β-thalassemia mutations and β-globin gene polymorphisms with DNA polymorphisms in the human β-globin gene cluster
12. Notes on geographical distribution and probable affinities
13. HinfI polymorphism 3′ to the human β-globin gene detected by the polymerase chain reaction (PCR)
14. Heamoglobinopathies in India
15. Analysis of β-globin gene haplotypes in Asian Indians: Origin and spread of β-thalassemia on the Indian subcontinent
16. Tribes of India