Holoprosencephaly in deletions of proximal chromosome 14q

J Med Genet. 1998 Jul;35(7):612. doi: 10.1136/jmg.35.7.612.
No abstract available

Publication types

  • Letter
  • Review

MeSH terms

  • Animals
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 14 / genetics*
  • Holoprosencephaly / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Mice
  • Mice, Knockout
  • Nuclear Proteins / genetics
  • Phenotype
  • Thyroid Nuclear Factor 1
  • Transcription Factors / genetics

Substances

  • Nuclear Proteins
  • Thyroid Nuclear Factor 1
  • Transcription Factors