Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant

MLA

Kheloud M. Alhamoudi, et al. “Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant.” Frontiers in Genetics, vol. 13, July 2022. EBSCOhost, https://doi.org/10.3389/fgene.2022.885589.

APA

Kheloud M. Alhamoudi, Balgees Alghamdi, Abeer Aljomaiah, Meshael Alswailem, Hindi Al-Hindi, & Ali S. Alzahrani. (2022). Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.885589

Chicago

Kheloud M. Alhamoudi, Balgees Alghamdi, Abeer Aljomaiah, Meshael Alswailem, Hindi Al-Hindi, and Ali S. Alzahrani. 2022. “Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant.” Frontiers in Genetics 13 (July). doi:10.3389/fgene.2022.885589.