[18 p-syndrome and hypothyroidism]

Arch Fr Pediatr. 1973 May;30(5):548.
[Article in French]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Chromosome Aberrations*
  • Chromosome Disorders*
  • Chromosomes, Human, 16-18*
  • Dermatoglyphics
  • Female
  • Humans
  • Hypothyroidism / complications*
  • Karyotyping