A de novo 1.9-Mb interstitial deletion of 3q13.2q13.31 in a girl with dysmorphic features, muscle hypotonia, and developmental delay

Am J Med Genet A. 2009 Aug;149A(8):1818-22. doi: 10.1002/ajmg.a.32963.
No abstract available

Publication types

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

MeSH terms

  • Base Pairing / genetics*
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 3 / genetics*
  • Comparative Genomic Hybridization
  • Developmental Disabilities / complications*
  • Developmental Disabilities / genetics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Muscle Hypotonia / complications*
  • Muscle Hypotonia / genetics*
  • Physical Chromosome Mapping