Spontaneous mutation in man

Adv Hum Genet. 1975:5:223-318. doi: 10.1007/978-1-4615-9068-2_4.
No abstract available

Publication types

  • Review

MeSH terms

  • Abnormalities, Multiple / genetics
  • Age Factors
  • Angiomatosis / genetics
  • Animals
  • Bone Diseases, Developmental / genetics
  • Chromosome Aberrations / genetics
  • Chromosome Disorders
  • Female
  • Genes, Dominant
  • Genes, Recessive
  • Genetic Code
  • Genetics, Medical*
  • Genetics, Microbial
  • Hemoglobins
  • Hemophilia A / genetics
  • Humans
  • Intestinal Polyps / genetics
  • Male
  • Mice
  • Models, Biological
  • Mosaicism
  • Muscular Dystrophies / genetics
  • Mutation*
  • Neurofibromatosis 1 / genetics
  • Oogenesis
  • Pigmentation Disorders / genetics
  • Polycystic Kidney Diseases / genetics
  • Probability
  • Retinoblastoma / genetics
  • Sex Chromosomes
  • Species Specificity
  • Spermatogenesis
  • Syndrome
  • Tuberous Sclerosis / genetics

Substances

  • Hemoglobins