Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Lignende værker

• Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  af: Kim, Hyung-Goo, et al.
  Udgivet: (2008)
• WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  af: Kim, Hyung-Goo, et al.
  Udgivet: (2010)
• WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
  af: Hyung‐Goo Kim, et al.
  Udgivet: (2010)
• 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: Ning Xu, et al.
  Udgivet: (2011)