Clinical genetic testing for Kallmann syndrome

J Clin Endocrinol Metab. 2013 May;98(5):1860-2. doi: 10.1210/jc.2013-1624.
No abstract available

Publication types

  • Editorial
  • Research Support, N.I.H., Extramural
  • Comment

MeSH terms

  • DNA Helicases / genetics*
  • DNA-Binding Proteins / genetics*
  • Extracellular Matrix Proteins / genetics*
  • Female
  • Fibroblast Growth Factor 8 / genetics*
  • Humans
  • Kallmann Syndrome / genetics*
  • Male
  • Mutation*
  • Nerve Tissue Proteins / genetics*
  • Polymorphism, Genetic*
  • Receptor, Fibroblast Growth Factor, Type 1 / genetics*

Substances

  • ANOS1 protein, human
  • DNA-Binding Proteins
  • Extracellular Matrix Proteins
  • FGF8 protein, human
  • Nerve Tissue Proteins
  • Fibroblast Growth Factor 8
  • FGFR1 protein, human
  • Receptor, Fibroblast Growth Factor, Type 1
  • DNA Helicases
  • CHD7 protein, human