[Pure ovarian dysgenesis with translocation t (X;3) (q21;q12) (author's transl)]

Ann Pediatr (Paris). 1980 Feb;27(2):129-32.
[Article in French]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Chromosome Aberrations / diagnosis
  • Chromosome Disorders
  • Chromosomes, Human, 1-3
  • Female
  • Gonadal Dysgenesis / genetics*
  • Humans
  • Ovary / abnormalities
  • Translocation, Genetic
  • X Chromosome