Correa Brito, L.; Grinspon, R.P.; Lopez Dacal, J.; Scaglia, P.; Esnaola Azcoiti, M.; Izquierdo, A.; Ropelato, M.G.; Rey, R.A.
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. J. Pers. Med. 2023, 13, 1158.
https://doi.org/10.3390/jpm13071158
AMA Style
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
Chicago/Turabian Style
Correa Brito, Lourdes, Romina P. Grinspon, Jimena Lopez Dacal, Paula Scaglia, MarÃa Esnaola Azcoiti, AgustÃn Izquierdo, MarÃa 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
APA Style
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
