Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly

J Med Genet. 2002 Oct;39(10):E60. doi: 10.1136/jmg.39.10.e60.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Chromosomes, Human, Pair 19 / genetics*
  • Gene Duplication*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Karyotyping / methods
  • Male
  • Microcephaly / genetics*
  • Psychomotor Disorders / genetics
  • Telomere / genetics*