Clinical utility gene card for: Mowat-Wilson syndrome

Eur J Hum Genet. 2011 Aug;19(8). doi: 10.1038/ejhg.2011.12. Epub 2011 Feb 23.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Human, Pair 2
  • Facies
  • Hirschsprung Disease / diagnosis
  • Hirschsprung Disease / genetics*
  • Hirschsprung Disease / physiopathology
  • Homeodomain Proteins / genetics*
  • Humans
  • Intellectual Disability / diagnosis
  • Intellectual Disability / genetics*
  • Intellectual Disability / physiopathology
  • Microcephaly / diagnosis
  • Microcephaly / genetics*
  • Microcephaly / physiopathology
  • Repressor Proteins / genetics*
  • Zinc Finger E-box Binding Homeobox 2

Substances

  • Homeodomain Proteins
  • Repressor Proteins
  • ZEB2 protein, human
  • Zinc Finger E-box Binding Homeobox 2

Supplementary concepts

  • Mowat-Wilson syndrome