Prenatal diagnosis of severe factor VII deficiency using mutation detection and linkage analysis

Br J Haematol. 2001 Jan;112(1):251-2. doi: 10.1046/j.1365-2141.2001.02497-4.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Chromosome Mapping
  • DNA Mutational Analysis
  • Female
  • Fetal Diseases / diagnosis*
  • Hemophilia A / diagnosis*
  • Humans
  • Infant, Newborn
  • Pregnancy
  • Prenatal Diagnosis / methods*