Works matching IS 20908571 AND DT 2021 AND VI 10 AND IP 1
Results: 9
Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Fragile X syndrome clinical and associated comorbidities.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Clinical report of Roifman syndrome with vitamin D-dependent rickets – an undocumented association.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Erratum: Lymphocyte mosaicism in Fanconi anemia: diagnosis and clinical correlation.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Chromosome therapy: different approaches and current challenges.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Black Immunity: Racial discrimination or genetic susceptibility?
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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Association of epidermal growth factor genotype with angiogenesis in Egyptian hepatocellular carcinoma and cirrhotic patients.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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- Article