Absence of SIX3 mutations in patients with congenital hypopituitarism

Am J Med Genet A. 2009 Dec;149A(12):2874-6. doi: 10.1002/ajmg.a.33103.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Human, Pair 2 / genetics
  • Cohort Studies
  • Eye Proteins / genetics*
  • Female
  • Homeobox Protein SIX3
  • Homeodomain Proteins / genetics*
  • Humans
  • Hypopituitarism / congenital*
  • Hypopituitarism / genetics*
  • Male
  • Mutation / genetics*
  • Nerve Tissue Proteins / genetics*
  • Polymorphism, Single Nucleotide / genetics

Substances

  • Eye Proteins
  • Homeodomain Proteins
  • Nerve Tissue Proteins