Found: 7
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Diagnostic value of molecular approach in screening for fragile X premutation cases.
- Published in:
- Irish Journal of Medical Science, 2023, v. 192, n. 5, p. 2265, doi. 10.1007/s11845-022-03166-9
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- Article
Whole exome screening of neurodevelopmental regression disorders in a cohort of Egyptian patients.
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- Neurogenetics, 2023, v. 24, n. 1, p. 17, doi. 10.1007/s10048-022-00703-7
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- Article
Fragile X syndrome clinical and associated comorbidities.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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- Article
Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.
- Published in:
- 2022
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- Correction Notice
Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.
- Published in:
- Journal of Genetic Engineering & Biotechnology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s43141-022-00399-0
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- Article
Correlation of circulating miRNA-33a and miRNA-122 with lipid metabolism among Egyptian patients with metabolic syndrome.
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- Journal of Genetic Engineering & Biotechnology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s43141-021-00246-8
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- Publication type:
- Article
The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 5, p. 4413, doi. 10.1007/s11033-021-06459-x
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- Article