Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome

J Med Genet. 2003 Aug;40(8):601-5. doi: 10.1136/jmg.40.8.601.
No abstract available

Publication types

  • Multicenter Study
  • Comment

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Agenesis of Corpus Callosum
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Face / abnormalities
  • Female
  • Genotype
  • Heart Defects, Congenital / genetics*
  • Hirschsprung Disease / genetics*
  • Homeodomain Proteins / genetics*
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Male
  • Phenotype
  • Repressor Proteins / genetics*
  • Seizures / genetics*
  • Syndrome
  • Toes / abnormalities
  • Zinc Finger E-box Binding Homeobox 2
  • Zinc Fingers / genetics

Substances

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