A novel presentation of a rare chromosome 2p25.2 deletion

Clin Dysmorphol. 2010 Apr;19(2):101-102. doi: 10.1097/MCD.0b013e328337bb28.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 2 / genetics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Pregnancy