Identification of a de novo 46, XY,4p+ with incomplete Wolf-Hirschhorn syndrome as 46,XY,der(4)t(4;8)(p16.3;p23.1)

Genet Couns. 1998;9(2):157-8.
No abstract available

Publication types

  • Letter

MeSH terms

  • Abnormalities, Multiple
  • Chromosome Aberrations*
  • Chromosome Disorders*
  • Chromosomes, Human, Pair 4*
  • Chromosomes, Human, Pair 8*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Syndrome
  • Translocation, Genetic*
  • Trisomy