Skip to main content
PMC home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1988 May;42(5):651–662.

Prevalence of genetic and partially genetic diseases in man and the estimation of genetic risks of exposure to ionizing radiation.

K Sankaranarayanan 1
PMCID: PMC1715178  PMID: 3282435

Full text

PDF
651

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alexander M L. Mutation Rates at Specific Autosomal Loci in the Mature and Immature Germ Cells of Drosophila Melanogaster. Genetics. 1954 May;39(3):409–428. doi: 10.1093/genetics/39.3.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baird P. A., Anderson T. W., Newcombe H. B., Lowry R. B. Genetic disorders in children and young adults: a population study. Am J Hum Genet. 1988 May;42(5):677–693. [PMC free article] [PubMed] [Google Scholar]
  3. Brent R. L. The complexities of solving the problem of human malformations. Clin Perinatol. 1986 Sep;13(3):491–503. [PubMed] [Google Scholar]
  4. Carter C. O. Genetics of common single malformations. Br Med Bull. 1976 Jan;32(1):21–26. doi: 10.1093/oxfordjournals.bmb.a071318. [DOI] [PubMed] [Google Scholar]
  5. Crow J. F., Denniston C. The mutation component of genetic damage. Science. 1981 May 22;212(4497):888–893. doi: 10.1126/science.7233180. [DOI] [PubMed] [Google Scholar]
  6. Czeizel A., Sankaranarayanan K. The load of genetic and partially genetic disorders in man. I. Congenital anomalies: estimates of detriment in terms of years of life lost and years of impaired life. Mutat Res. 1984 Aug;128(1):73–103. doi: 10.1016/0027-5107(84)90049-6. [DOI] [PubMed] [Google Scholar]
  7. Denniston C. Low level radiation and genetic risk estimation in man. Annu Rev Genet. 1982;16:329–355. doi: 10.1146/annurev.ge.16.120182.001553. [DOI] [PubMed] [Google Scholar]
  8. Edwards J. H. The mutation rate in man. Prog Med Genet. 1974;10:1–16. [PubMed] [Google Scholar]
  9. Kalter H., Warkany J. Medical progress. Congenital malformations: etiologic factors and their role in prevention (first of two parts). N Engl J Med. 1983 Feb 24;308(8):424–431. doi: 10.1056/NEJM198302243080804. [DOI] [PubMed] [Google Scholar]
  10. Kline J., Stein Z. Environmental causes of aneuploidy: why so elusive? Basic Life Sci. 1985;36:149–164. doi: 10.1007/978-1-4613-2127-9_10. [DOI] [PubMed] [Google Scholar]
  11. Lüning K. G., Searle A. G. Estimates of the genetic risks from ionizing irradiation. Mutat Res. 1971 Jul;12(3):291–304. doi: 10.1016/0027-5107(71)90017-0. [DOI] [PubMed] [Google Scholar]
  12. Neel J. V., Satoh C., Goriki K., Asakawa J., Fujita M., Takahashi N., Kageoka T., Hazama R. Search for mutations altering protein charge and/or function in children of atomic bomb survivors: final report. Am J Hum Genet. 1988 May;42(5):663–676. [PMC free article] [PubMed] [Google Scholar]
  13. RUSSELL W. L. X-ray-induced mutations in mice. Cold Spring Harb Symp Quant Biol. 1951;16:327–336. doi: 10.1101/sqb.1951.016.01.024. [DOI] [PubMed] [Google Scholar]
  14. Sankaranarayanan K. The role of non-disjunction in aneuploidy in man. An overview. Mutat Res. 1979 Jun;61(1):1–28. doi: 10.1016/0027-5107(79)90003-4. [DOI] [PubMed] [Google Scholar]
  15. Schull W. J., Otake M., Neel J. V. Genetic effects of the atomic bombs: a reappraisal. Science. 1981 Sep 11;213(4513):1220–1227. doi: 10.1126/science.7268429. [DOI] [PubMed] [Google Scholar]
  16. Shokeir M. H. Investigations on Huntington's disease in the Canadian Prairies. I. Prevalence. Clin Genet. 1975 Apr;7(4):345–348. doi: 10.1111/j.1399-0004.1975.tb00340.x. [DOI] [PubMed] [Google Scholar]
  17. Straume T., Dobson R. L., Kwan T. C. Neutron RBEs and the radiosensitive target for mouse immature oocyte killing. Radiat Res. 1987 Jul;111(1):47–57. [PubMed] [Google Scholar]
  18. Sutton H. E. The impact of induced mutations on human populations. Mutat Res. 1975 Nov;33(1 Spec No):17–24. doi: 10.1016/0027-5107(75)90038-x. [DOI] [PubMed] [Google Scholar]
  19. Trimble B. K., Doughty J. H. The amount of hereditary disease in human populations. Ann Hum Genet. 1974 Oct;38(2):199–223. doi: 10.1111/j.1469-1809.1974.tb01951.x. [DOI] [PubMed] [Google Scholar]
  20. Vogel F. Clinical consequences of heterozygosity for autosomal-recessive diseases. Clin Genet. 1984 May;25(5):381–415. [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES