Order Article Reprints

Correa Brito L, Grinspon RP, Lopez Dacal J, Scaglia P, Esnaola Azcoiti M, Izquierdo A, Ropelato MG, Rey RA. Identification of a Novel Variant in Myelin Regulatory Growth Factor by Next-Generation Sequencing Led to the Detection of a Clinically Inapparent Congenital Heart Defect in a Patient with a 46,XY Disorder of Sex Development. Journal of Personalized Medicine. 2023; 13(7):1158. https://doi.org/10.3390/jpm13071158

Correa Brito, Lourdes, Romina P. Grinspon, Jimena Lopez Dacal, Paula Scaglia, María Esnaola Azcoiti, Agustín Izquierdo, María Gabriela Ropelato, and Rodolfo A. Rey. 2023. "Identification of a Novel Variant in Myelin Regulatory Growth Factor by Next-Generation Sequencing Led to the Detection of a Clinically Inapparent Congenital Heart Defect in a Patient with a 46,XY Disorder of Sex Development" Journal of Personalized Medicine 13, no. 7: 1158. https://doi.org/10.3390/jpm13071158

Correa Brito, L., Grinspon, R. P., Lopez Dacal, J., Scaglia, P., Esnaola Azcoiti, M., Izquierdo, A., Ropelato, M. G., & Rey, R. A. (2023). Identification of a Novel Variant in Myelin Regulatory Growth Factor by Next-Generation Sequencing Led to the Detection of a Clinically Inapparent Congenital Heart Defect in a Patient with a 46,XY Disorder of Sex Development. Journal of Personalized Medicine, 13(7), 1158. https://doi.org/10.3390/jpm13071158