Clinical, endocrinological, and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence

Documenti analoghi

• Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience
  di: Shin, Sun-Jeong, et al.
  Pubblicazione: (2015)
• The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome
  di: Quaynor, Samuel D., et al.
  Pubblicazione: (2011)
• Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism
  di: Pitteloud, Nelly, et al.
  Pubblicazione: (2007)
• Dizygotic twin sisters with normosmic idiopathic hypogonadotropic hypogonadism caused by an gene variant
  di: Jaewon Choe, et al.
  Pubblicazione: (2020-07-01)
• Nasal Embryonic LHRH Factor (NELF) Mutations in Patients with Normosmic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  di: Xu, Ning, et al.
  Pubblicazione: (2011)