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Vrečar I, Innes J, Jones EA, et al. Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Absent Speech, and Involuntary Movements. J Pediatr Genet. 2017;6(3):129-141doi: 10.1055/s-0037-1601335.
Vrečar, I., Innes, J., Jones, E. A., Kingston, H., Reardon, W., Kerr, B., Clayton-Smith, J., & Douzgou, S. (2017). Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Absent Speech, and Involuntary Movements. Journal of pediatric genetics, 6(3), 129-141. https://doi.org/10.1055/s-0037-1601335
Vrečar, Irena, et al. "Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Absent Speech, and Involuntary Movements." Journal of pediatric genetics vol. 6,3 (2017): 129-141. doi: https://doi.org/10.1055/s-0037-1601335
Vrečar I, Innes J, Jones EA, Kingston H, Reardon W, Kerr B, Clayton-Smith J, Douzgou S. Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Absent Speech, and Involuntary Movements. J Pediatr Genet. 2017 Sep;6(3):129-141. doi: 10.1055/s-0037-1601335. Epub 2017 Apr 12. PMID: 28794905; PMCID: PMC5548525.
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