An uncommon case of a female carrier of two distinct X-linked disorders

Haemophilia. 2008 May;14(3):665-6. doi: 10.1111/j.1365-2516.2008.01665.x. Epub 2008 Feb 15.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Charcot-Marie-Tooth Disease / genetics*
  • Female
  • Genetic Counseling
  • Genetic Diseases, X-Linked*
  • Hemophilia A / genetics*
  • Humans
  • Male
  • Mutation / genetics
  • Pedigree
  • Pregnancy
  • Prenatal Diagnosis