Fazeli, Z., Ghaderian, S. M. H., Najmabadi, H. and Omrani, M. D. (2022) “Understanding the Molecular Basis of Fragile X Syndrome Using Differentiated Mesenchymal Stem Cells”, Iranian Journal of Child Neurology, 16(1), pp. 85–95. doi: 10.22037/ijcn.v15i4.22070.