Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families

Am J Med Genet A. 2012 Jan;158A(1):254-6. doi: 10.1002/ajmg.a.34378. Epub 2011 Nov 21.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 7 / genetics*
  • Female
  • Forkhead Transcription Factors / genetics*
  • Genetic Loci
  • Genotype
  • Humans
  • Infant
  • Inheritance Patterns*
  • Male
  • Pedigree

Substances

  • FOXP2 protein, human
  • Forkhead Transcription Factors