Ring chromosome 13 in an infant with multiple congenital anomalies and penoscrotal transposition

Clin Dysmorphol. 1998 Oct;7(4):299-301. doi: 10.1097/00019605-199810000-00012.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Anus, Imperforate / genetics
  • Chromosomes, Human, Pair 13 / genetics*
  • Humans
  • Infant
  • Male
  • Penis / abnormalities*
  • Ring Chromosomes*
  • Scrotum / abnormalities*
  • Syndrome