An (X;1) translocation, balanced, 46 chromosomes. Repository identification no. GM-97

Cytogenet Cell Genet. 1974;13(4):406-7. doi: 10.1159/000130291.
No abstract available

MeSH terms

  • Abnormalities, Multiple / genetics
  • Cells, Cultured*
  • Chromosome Aberrations*
  • Chromosomes, Human, 1-3*
  • Female
  • Genetic Linkage
  • Hernia, Umbilical / congenital
  • Humans
  • Infant
  • Karyotyping
  • Sex Chromosomes*
  • Skin / ultrastructure
  • Staining and Labeling
  • Syndrome
  • Tongue / abnormalities
  • Translocation, Genetic*