Isolated hypermethylation of GRB10 (7p12.2) in a Silver-Russell syndrome patient carrying a 20p13 microdeletion

Clin Genet. 2014 Apr;85(4):399-400. doi: 10.1111/cge.12186. Epub 2013 Jun 10.
No abstract available

Publication types

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

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 20*
  • DNA Methylation
  • GRB10 Adaptor Protein / genetics*
  • GRB10 Adaptor Protein / metabolism
  • Humans
  • Male
  • Silver-Russell Syndrome / genetics*

Substances

  • GRB10 protein, human
  • GRB10 Adaptor Protein