Partial iris hypoplasia in a patient with an interstitial subtelomeric 6p deletion not including the forkhead transcription factor gene FOXC1

Eur J Hum Genet. 2005 Nov;13(11):1169-71. doi: 10.1038/sj.ejhg.5201487.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 6*
  • Female
  • Forkhead Transcription Factors / genetics*
  • Humans
  • Infant
  • Iris / abnormalities*
  • Physical Chromosome Mapping
  • Telomere

Substances

  • Forkhead Transcription Factors