The identification of HESX1 mutations in Kallmann syndrome

Lignende værker

• The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome
  af: Quaynor, Samuel D., 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)
• Nasal Embryonic LHRH Factor (NELF) Mutations in Patients with Normosmic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  af: Xu, Ning, et al.
  Udgivet: (2011)
• The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
  af: Pedersen-White, Jennifer R., et al.
  Udgivet: (2008)
• Clinical Genetic Testing for Kallmann Syndrome
  af: Layman, Lawrence C.
  Udgivet: (2013)