Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience

समान संसाधन

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