A role for the otolaryngologist in identification and discovery of genetic disorders and chromosomal abnormalities

Arch Otolaryngol Head Neck Surg. 1993 Oct;119(10):1074-81. doi: 10.1001/archotol.1993.01880220018005.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Child, Preschool
  • Chromosome Aberrations / diagnosis*
  • Chromosome Aberrations / genetics
  • Chromosome Disorders
  • Diagnosis, Differential
  • Female
  • Genetic Diseases, Inborn / diagnosis*
  • Genetic Diseases, Inborn / genetics
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Otolaryngology*