Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient

Am J Med Genet. 1995 Nov 20;59(3):406-7. doi: 10.1002/ajmg.1320590332.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Cell Line, Transformed
  • Cells, Cultured
  • Chromosome Aberrations / genetics*
  • Chromosome Deletion*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 17 / genetics
  • Chromosomes, Human, Pair 17 / ultrastructure*
  • Cosmids
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence*
  • Lymphocytes / ultrastructure
  • Male
  • Mosaicism / genetics*
  • Syndrome