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Molecular Genetics & Genomic Medicine|January 25, 2017
Genetics and Genomic Medicine in Egypt: steady paceSamia Ali Temtamy, Dalia Farouk HussenAmerican Journal of Medical Genetics. Part A|June 28, 2023
Clinical and molecular characterization in a cohort of patients with progressive pseudorheumatoid dysplasiaDina El Dessouki, Khalda Amr, Naglaa Kholoussi, et al.BMC Genomics|September 9, 2024
Biallelic TYR and TKFC variants in Egyptian patients with OCA1 and new expanded TKFC featuresEngy A Ashaat, Nora N Esmaiel, Sonia A El-Saiedi, et al.Molecular Neurobiology|December 28, 2023
The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar AtrophyEngy A Ashaat, Hoda A Ahmed, Nesma M Elaraby, et al.American Journal of Medical Genetics. Part A|September 28, 2020
Rubinstein-Taybi syndrome in diverse populationsCedrik Tekendo-Ngongang, Babajide Owosela, Nicole Fleischer, et al.American Journal of Medical Genetics. Part A|December 20, 2019
Turner syndrome in diverse populationsPaul Kruszka, Yonit A Addissie, Cedrik Tekendo-Ngongang, et al.American Journal of Medical Genetics. Part A|April 23, 2018
Williams-Beuren syndrome in diverse populationsPaul Kruszka, Antonio R Porras, Deise Helena de Souza, et al.Pageof 1