The novel p.Cys65Tyr mutation in NR5A1gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency

Míreanna comhchosúla

• The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency
  de réir: Fabbri, Helena Campos, et al.
  Foilsithe / Cruthaithe: (2014)
• Molecular Diagnosis of 5α-Reductase Type II Deficiency in Brazilian Siblings with 46,XY Disorder of Sex Development
  de réir: de Calais, Flávia Leme, et al.
  Foilsithe / Cruthaithe: (2011)
• Molecular Diagnosis of 5α-Reductase Type II Deficiency in Brazilian Siblings with 46,XY Disorder of Sex Development
  de réir: Flávia Leme de Calais, et al.
  Foilsithe / Cruthaithe: (2011)
• DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis
  de réir: Felipe Rodrigues de Oliveira, et al.
  Foilsithe / Cruthaithe: (2023)
• Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Reared as Males
  de réir: Juliana Gabriel Ribeiro de Andrade, et al.
  Foilsithe / Cruthaithe: (2014)