A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome

Am J Med Genet A. 2009 Aug;149A(8):1842-5. doi: 10.1002/ajmg.a.32980.
No abstract available

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Base Pairing / genetics
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 13 / genetics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Oligonucleotide Array Sequence Analysis
  • Syndrome
  • Young Adult