Atypical deletion in Williams-Beuren syndrome critical region detected by MLPA in a patient with supravalvular aortic stenosis and learning difficulty

J Genet Genomics. 2012 Oct 20;39(10):571-4. doi: 10.1016/j.jgg.2012.07.001. Epub 2012 Jul 31.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aortic Stenosis, Supravalvular / complications*
  • Gene Deletion*
  • Humans
  • Learning Disabilities / complications*
  • Male
  • Nucleic Acid Amplification Techniques*
  • Phenotype
  • Williams Syndrome / complications*
  • Williams Syndrome / genetics*
  • Young Adult