Campomelic syndrome in phenotypic females with 46,XY chromosomes: evidence of genetic heterogeneity

Clin Pediatr (Phila). 1981 Mar;20(3):214-6. doi: 10.1177/000992288102000308.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple
  • Dwarfism / genetics*
  • Female
  • Gonadal Dysgenesis / genetics*
  • Gonadal Dysgenesis, 46,XY / genetics*
  • Humans
  • Infant, Newborn
  • Karyotyping