Familial occurrence of a del(Xp-) chromosome: pitfall in karyotype/phenotype correlation

Am J Med Genet. 1998 Dec 4;80(4):436-8. doi: 10.1002/(sici)1096-8628(19981204)80:4<436::aid-ajmg26>3.0.co;2-4.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Chromosome Deletion*
  • Family Health
  • Female
  • Humans
  • Karyotyping
  • Male
  • Pedigree
  • Phenotype
  • Turner Syndrome / genetics
  • Turner Syndrome / pathology
  • X Chromosome / genetics*