Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration-Reference-Cited by-同舟云学术

Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration

Published:2005-01 Issue:1 Volume:69 Page:55-66
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Makhoul N. J.¹,Wells R. S.²,Kaspar H.¹³,Shbaklo H.³,Taher A.¹⁴,Chakar N.¹,Zalloua P. A.¹⁵

Affiliation:

1. Department of Obstetrics and Gynecology, American University of Beirut, Beirut, Lebanon

2. Oxford University, London, UK

3. Genetics Research Laboratory, Chronic Care Center, Beirut, Lebanon

4. Department of Internal Medicine, American University of Beirut, Beirut, Lebanon

5. Program for Population Genetics, Harvard School of Public Health, Boston, USA

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1529-8817.2004.00138.x

Reference43 articles.

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3. Sickle cell anemia, sickle cell beta‐thalassemia, and thalassemia major in Albania: characterization of mutations;Boletini E.;Hum Genet,1994

4. Anthropological approach to the heterogeneity of beta‐thalassemia mutations in Northern Africa;Bennani C.;Hum Biol,1994

5. [Detection of beta thalassemia by the technique of refractory amplification of mutation systems (ARMS‐PCR)];Bravo M.;Invest Clin,1999

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