46 XX Ovotesticular Disorder of Sex Development with Gonadotropin-Releasing Hormone Receptor, Autosomal Recessive Heterozygous Missense Mutation and Autosomal Dominant Heterozygous Missense Mutation of the PROKR2 Gene: A Case Report.

Autor: Peranzoni F; Department of Pediatric Surgery, Lausanne University Hospital, Lausanne, Switzerland., De Castro R; Thien Nhan and Friends Association, Italy., Merlini E; Department of Pediatric Surgery, Hospital of Alexandria, Italy., Nguyen YL; Department of Pediatric Urology, Vietnam National Hospital of Pediatric 2, Ho Chi Minh City, Vietnam.

Publikováno v: Global medical genetics [Glob Med Genet] 2024 Jul 09; Vol. 11 (3), pp. 220-224. Date of Electronic Publication: 2024 Jul 09 (Print Publication: 2024).