The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Lignende værker

• The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
  af: Pedersen-White, Jennifer R., et al.
  Udgivet: (2008)
• Nasal Embryonic LHRH Factor (NELF) Mutations in Patients with Normosmic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  af: Xu, Ning, et al.
  Udgivet: (2011)
• The Role of CHD7 Mutations in Patients with Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  af: Kim, Hyung-Goo, et al.
  Udgivet: (2011)
• GNRHR biallelic and digenic mutations in patients with normosmic congenital hypogonadotropic hypogonadism
  af: Gonçalves, Catarina I, et al.
  Udgivet: (2017)
• Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  af: Kim, Hyung-Goo, et al.
  Udgivet: (2008)