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Journal: Journal of Personalized MedicineVolume: 13Number: 1158
Article: 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
  • Authors:
  • Lourdes Correa Brito1,
  • Romina P. Grinspon1 and
  • Jimena Lopez Dacal1
  • et al.
Link: https://www.mdpi.com/2075-4426/13/7/1158

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