Prenatal genetic diagnosis. 3

N Engl J Med. 1970 Dec 31;283(27):1498-504. doi: 10.1056/NEJM197012312832705.
No abstract available

Publication types

  • Review

MeSH terms

  • Abortion, Induced
  • Acid Phosphatase / metabolism
  • Adrenal Hyperplasia, Congenital / diagnosis
  • Amnion
  • Amniotic Fluid / analysis
  • Carbohydrate Metabolism, Inborn Errors / diagnosis
  • Congenital Abnormalities / diagnosis
  • Counseling
  • Culture Techniques
  • Cystic Fibrosis / diagnosis
  • Economics, Medical
  • Ethics, Medical
  • Female
  • Fetal Diseases / diagnosis*
  • Fibroblasts / cytology
  • Fibroblasts / enzymology
  • Genetic Diseases, Inborn / diagnosis*
  • Glycogen Storage Disease / diagnosis
  • Heterozygote
  • Homozygote
  • Humans
  • Lysosomes / enzymology
  • Mannose
  • Marfan Syndrome / diagnosis
  • Methods
  • Mucopolysaccharidoses / diagnosis
  • Muscular Dystrophies / diagnosis
  • Porphyrias / diagnosis
  • Pregnancy
  • Punctures
  • Xeroderma Pigmentosum / diagnosis

Substances

  • Acid Phosphatase
  • Mannose