[Ring chromosome 18. 18p-/18q- -deletion-syndrome]

Humangenetik. 1972;15(4):289-318. doi: 10.1007/BF00281730.
[Article in German]
No abstract available

Publication types

  • Review

MeSH terms

  • Abnormalities, Multiple
  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Aberrations*
  • Chromosome Disorders*
  • Chromosomes, Human, 16-18*
  • Craniofacial Dysostosis / genetics
  • Deafness / genetics
  • Female
  • Heart Defects, Congenital / genetics
  • Humans
  • Hypotension / genetics
  • Infant
  • Infant, Newborn
  • Karyotyping
  • Male
  • Microcephaly / genetics
  • Middle Aged
  • Mitosis
  • Muscular Diseases / genetics
  • Phenotype
  • Psychomotor Disorders / genetics
  • Syndrome