Robins's syndrome in three children of consanguineous parents. A pedigree suggesting autosomal recessive inheritance

Acta Genet Med Gemellol (Roma). 1972 Oct;21(4):349-53. doi: 10.1017/s0001566000010710.
No abstract available

MeSH terms

  • Consanguinity
  • Female
  • Genes, Recessive*
  • Humans
  • Infant, Newborn
  • Male
  • Pedigree
  • Pierre Robin Syndrome / genetics*