β-Thalassemia mutations and haplotype analysis in Lebanon

Hemoglobin

Volumn 24, Issue 4, 2000, Pages 269-276

  Zahed, L ^a   Qatanani, M ^a   Nabulsi, M ^a   Taher, A ^a  

^a AMERICAN UNIVERSITY OF BEIRUT   (Lebanon)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BETA THALASSEMIA; CHROMOSOME ANALYSIS; CONTROLLED STUDY; GENE AMPLIFICATION; GENE CLUSTER; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GEOGRAPHY; HAPLOTYPE; HUMAN; LEBANON; POLYMERASE CHAIN REACTION; RELIGION; RESTRICTION SITE;

EID: 0033693877     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630260008993133     Document Type: Article

References (15)

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5. Analysis of β-globin gene haplotypes in Asian Indians: Origin and spread of β-thalassemia on the Indian subcontinent
6. β-Thalassemia mutations and their linkage to β-haplotypes in Tamilnadu in Southern India
7. Thalassemia in Lebanon
8. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
9. Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants
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11. Anthropological approach to the heterogeneity of β-thalassemia mutations in Northern Africa
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14. Major β-globin gene mutations in eastern India and their associated haplotypes
15. The β- and δ-thalassemia repository