Pachygyria and cerebellar hypoplasia in a patient with a 2q22-q23 deletion that includes the ZFHX1B gene

Am J Med Genet A. 2004 May 15;127A(1):109. doi: 10.1002/ajmg.a.20607.
No abstract available

Publication types

  • Letter

MeSH terms

  • Brain / abnormalities*
  • Cerebellum / abnormalities*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 2 / genetics*
  • Gene Deletion
  • Hirschsprung Disease / genetics*
  • Homeodomain Proteins / genetics*
  • Humans
  • Male
  • Repressor Proteins / genetics*
  • Syndrome
  • Zinc Finger E-box Binding Homeobox 2

Substances

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