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Connexin 26 Gene Mutations in Non-Syndromic Hearing Loss Among Kuwaiti Patients.
- Published in:
- Medical Principles & Practice, 2013, v. 23, n. 1, p. 74, doi. 10.1159/000348304
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- Article
Haemochromatosis gene mutation H63D is a risk factor for iron overload in Egyptian beta- thalassemic children.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 149
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- Article