Molecular characterisation of a supernumerary ring chromosome in a patient with VATER association

J Med Genet. 2001 Feb;38(2):E6. doi: 10.1136/jmg.38.2.e6.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Anus, Imperforate / pathology
  • Centromere / genetics
  • Chromosomes, Human, Pair 12 / genetics
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant, Newborn
  • Kidney / abnormalities
  • Male
  • Radius / abnormalities
  • Ring Chromosomes*
  • Spine / abnormalities