Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features

Clin Genet. 2012 Mar;81(3):298-300. doi: 10.1111/j.1399-0004.2011.01719.x. Epub 2011 Dec 28.
No abstract available

Publication types

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

MeSH terms

  • Alleles
  • Chromosomes, Human, Pair 7
  • Genomic Imprinting*
  • Humans
  • Male
  • Proteins / genetics*
  • Silver-Russell Syndrome / genetics*

Substances

  • Proteins
  • mesoderm specific transcript protein