A novel mutation in the SRY gene causing 46 XY complete gonadal dysgenesis in a Chinese patient

Ítems similars

• 46, XY complete gonadal dysgenesis with pubertal virilisation due to dysgerminoma/gonadoblastoma
  per: Alam, Sarah, et al.
  Publicat: (2020)
• A de novo frameshift mutation of the SRY gene leading to a patient with 46,XY complete gonadal dysgenesis
  per: Wang, Xiao-Bo, et al.
  Publicat: (2019)
• THE RISK FOR DEVELOPING TUMOR IN PATIENTS WITH GONADAL DYSGENESIS 46,XY
  per: O. Yu. Latyshev, et al.
  Publicat: (2015-10-01)
• 46 XY gonadal dysgenesis in adulthood ‘pitfalls of late diagnosis’
  per: Hamin, Jarna Naing, et al.
  Publicat: (2012)
• Imaging Findings in Dysgerminoma in a Case of 46 XY, Complete Gonadal Dysgenesis (Swyer syndrome)
  per: Yadav, Pratiksha, et al.
  Publicat: (2016)