Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean β‐thalassemia mutations
β‐Thalassemia is the most common genetic disorder in the Lebanese population. Of the 200 different mutations in the β‐globin gene that leads to thalassemia, the IVSI‐110 (29.87%), IVSI‐6 (20.74%), IVSI‐1 (14.07%), IVSII‐1 (9.13%), Cd29 (9.13%), and Cd30 (3.95%) mutations are the most frequent among...
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| Main Author: | Naja, R.P. (author) |
|---|---|
| Other Authors: | Kaspar, H. (author), Shbaklo, H. (author), Chakar, N. (author), Makhoul, N.J. (author), Zalloua, P.A. (author) |
| Format: | article |
| Published: |
2004
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| Online Access: | http://hdl.handle.net/10725/11113 https://doi.org/10.1002/ajh.20013 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://onlinelibrary.wiley.com/doi/abs/10.1002/ajh.20013 |
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