Identification of a submicroscopic deletion of SHH associated with the holoprosencephaly spectrum by array-based CGH

Clin Genet. 2006 Apr;69(4):367-9. doi: 10.1111/j.1399-0004.2006.00598.x.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Deletion*
  • Female
  • Hedgehog Proteins
  • Holoprosencephaly / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Oligonucleotide Array Sequence Analysis / methods
  • Trans-Activators / analysis
  • Trans-Activators / genetics*

Substances

  • Hedgehog Proteins
  • SHH protein, human
  • Trans-Activators