Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies

Am J Med Genet A. 2012 May;158A(5):1233-5. doi: 10.1002/ajmg.a.35305. Epub 2012 Apr 11.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Agenesis of Corpus Callosum / genetics
  • Child
  • Child, Preschool
  • Craniofacial Abnormalities
  • DNA-Binding Proteins / genetics*
  • Encephalocele / genetics
  • Eye Abnormalities / genetics
  • Face / abnormalities
  • Female
  • Homeodomain Proteins / genetics*
  • Humans
  • Infant
  • Mutation*
  • Repressor Proteins / genetics*
  • Syndrome
  • Transcription Factors / genetics*

Substances

  • ALX3 protein, human
  • ALX4 protein, human
  • DNA-Binding Proteins
  • Homeodomain Proteins
  • Repressor Proteins
  • TGIF1 protein, human
  • Transcription Factors

Supplementary concepts

  • Frontonasal dysplasia