Childhood monosomy 7: epidemiology, biology, and mechanistic implications

Blood. 1995 Apr 15;85(8):1985-99.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Aberrations / epidemiology
  • Chromosome Aberrations / genetics*
  • Chromosome Deletion*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 7*
  • Female
  • Genes, Neurofibromatosis 1
  • Genes, ras
  • Genetic Diseases, Inborn / genetics
  • Genetic Predisposition to Disease
  • Hematopoietic Stem Cells / pathology
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Leukemia, Myeloid / classification
  • Leukemia, Myeloid / epidemiology
  • Leukemia, Myeloid / genetics*
  • Leukemia, Myeloid / pathology
  • Leukemia, Radiation-Induced / genetics
  • Male
  • Monosomy*
  • Myelodysplastic Syndromes / classification
  • Myelodysplastic Syndromes / epidemiology
  • Myelodysplastic Syndromes / genetics*
  • Myelodysplastic Syndromes / pathology
  • Neoplasms, Second Primary / chemically induced
  • Neoplasms, Second Primary / etiology
  • Neoplasms, Second Primary / genetics
  • Risk