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Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy.
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- Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 1, p. 37, doi. 10.1016/j.ejmhg.2012.08.002
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- Article
Screening of GHSR, GHRHR, GH1 genes in isolated growth hormone deficiency disease in Egyptian patients.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00480-y
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- Article
Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls.
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- Egyptian Journal of Medical Human Genetics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s43042-023-00408-y
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- Article