[Dermatoglyphic changes of a familial nature associated with an inversion of the pair 1 chromosomes]

Rev Pediatr Obstet Ginecol Pediatr. 1988 Jul-Sep;37(3):261-5.
[Article in Romanian]
No abstract available

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosome Inversion*
  • Chromosomes, Human, Pair 1 / ultrastructure*
  • Dermatoglyphics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Premature