Genetic effects of ionising radiation in man

Awa A. A. Honda T. Neriishi S. Sofuni T. Shimba H. Ohtaki K. Nakano M. Kodama Y. Itoh M. Hamilton B. (1987). Cytogenetic study of the offspring of atomic bomb survivors, Hiroshima and Nagasaki. In: Cytogenetics: Basic and Applied Aspects, pp. 166–183 ( Obe G. Basler A. , eds). Springer, Berlin.

Baird P. A. Anderson T. W. Newcombe H. B. Lowry R. B. (1988). Genetic disorders in children and young adults: a population study. Am. J. Hum. Genet. 42, 677–693.

Bock G. Collins G. M. (eds) (1987). Molecular Approaches to Human Polygenic Disease. Ciba Foundation symposium 130, John Wiley & Sons Ltd, Chichester, U.K..

Brent R. L. (1986). The complexities of solving the problem of human malformations. In: Clinics in Perinatology, Vol. 13, pp. 491–503 ( Brent R. L. Beckman D. A. , eds). W. B. Saunders, Philadelphia.

Carter C. O. (1977). Monogenic disorders. J. Med. Genet. 14, 316–320.

Carter C. O. (1982). Contribution of gene mutations to genetic disease in humans. In: Progress in Mutation Research, Vol. 3, pp. 1–8 ( Bora K. C. Douglas G. R. Nestmann E. R. , eds). Elsevier Biomedical, Amsterdam.

Crow J. F. Denniston C. (1981). The mutation component of genetic damage. Science 212, 888–893.

Crow J. F. Denniston C. (1985). Mutation in human populations. In: Advances in Human Genetics, Vol. 14, pp. 59–123 ( Harris H. Hirschhorn K. , eds). Plenum Press, NY.

Czeizel A. (1989). Population surveillance of sentinel anomalies. Mutation Res. 212, 3–9.

Czeizel A. Sankaranarayanan K. (1984). 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. Mutation Res. 128, 73–103.

Czeizel A. Tusnady G. (1984). Aetiological Studies of Isolated Common Congenital Abnormalities in Hungary. Akademiai Kiado, Budapest.

Czeizel A. Vizkelety T. (1988). Hungarian birth prevalence of congenital dislocation of the hip in the Eighties. Orv. Hetil. 129, 2605.

Czeizel A. Sankaranarayanan K. Losonci A. Rudas T. Keresztes M. (1988). The load of genetic and partially genetic diseases in man. II. Some selected common multifactorial diseases: estimates of population prevalence and of detriment in terms of years of lost and impaired life. Mutation Res. 196, 259–292.

ICRP (1977). Recommendations of the International Commission on Radiological Protection , ICRP Publication 26. Annals of the ICRP 1(3). Pergamon Press, Oxford.

Kalter H. Warkany J. (1983). Congenital malformations: etiologic factors and their role in prevention. New Engl. J. Med. 308, 424–431.

Kline J. Stein Z. (1985). Environmental causes of aneuploidy: why so elusive? In: Aneuploidy: Etiology and Mechanisms, pp. 149–164 ( Dellarco V. L. Voytek P. E. Hollaender A. , eds). Plenum, New York.

NAS (1972). BEIR I Report. The Effects on Populations of Exposure to Low Levels of Ionizing Radiation. National Academy of Sciences, National Research Council, Washington, D.C..

NAS (1980). BEIR III Report. The Effects on Populations of Exposure to Low Levels of Ionizing Radiation. National Academy of Sciences, National Research Council, Washington, D.C..

NAS (1990). BEIR V Report. Health Effects of Exposure to Low Levels of Ionizing Radiation. National Academy of Sciences, National Research Council, Washington, D.C..

Neel J. V. Satoh C. Goriki K. Asakawa J. I. Fujita M. Takahashi N. Kageoka T. Hazama R. (1988). Search for mutations altering protein charge and/or function in children of atomic bomb survivors; final report. Am. J. Hum. Genet. 42, 663–676.

Neel J. V. Schull W. J. Awa A. A. Satoh C. Kato H. Otake M. Yoshimoto Y. (1990). The children of parents exposed to atomic bombs: estimates of the gametic doubling dose of radiation for humans. Am. J. Hum. Genet. 46, 1053–1072.

Nelson K. Holmes L. B. (1989). Malformations due to presumed spontaneous mutations in newborn infants. New Engl. J. Med. 320, 19–23.

Oftedal P. Searle A. G. (1980). An overall genetic risk assessment for radiological protection purposes. J. Med. Genet. 17, 15–20.

Otake M. Schull W. J. Neel J. V. (1990). Congenital malformations, stillbirths and early mortality among the children of atomic bomb survivors: a reanalysis. Radiat. Res. 122, 1–11.

Sankaranarayanan K. (1979). The role of non-disjunction in aneuploidy in man. Mutation Res. 61, 1–28.

Sankaranarayanan K. (1988). Invited review: prevalence of genetic and partially genetic diseases in man and the estimation of genetic risks of exposure to ionizing radiation. Am. J. Hum. Genet. 42, 651–662.

Sankaranarayanan K. (1990). Some problems and considerations in the assessment of genetic risks of exposure to ionizing radiation. In: Mutation and the Environment, Part C, pp. 233–245 ( Mendelsohn M. L. Albertini R. J. , eds). Wiley-Liss, NY.

Sankaranarayanan K. (1991a). Ionizing radiation and genetic risks. I. Epidemiological, population genetic, biochemical and molecular aspects of Mendelian diseases. Mutation Res., in press.

Sankaranarayanan K. (1991b). Ionizing radiation and genetic risks. II. Nature of radiation-induced mutations in experimental mammalian in vivo systems. Mutation Res., in press.

Sankaranarayanan K. (1991c). Ionizing radiation and genetic risks. III. Nature of spontaneous and radiation-induced mutations in mammalian in vitro systems and mechanisms of induction of mutations by radiation. Mutation Res., in press.

Sankaranarayanan K. (1991d). Ionizing radiation and genetic risks. IV. Current methods, estimates of risk of Mendelian disease, human data and lessons from biochemical and molecular studies of mutations. Mutation Res., in press.

Schull W. J. Neel J. V. Otake M. Awa A. Satoh C. Hamilton H. B. (1982). Hiroshima and Nagasaki: three and a half decades of genetic screening. In: Environmental Mutagens and Carcinogens, pp. 687–700 ( Sugimura T. Kondo S. , eds). Alan R. Liss, New York.

Scott J. (1987). Molecular genetics of common diseases. Brit. Med. J. 295, 769–771.

Stevenson A. C. (1959). The load of hereditary defects in human populations. Radiat. Res. (Suppl.) 1, 306–325.

Trimble B. K. Doughty J. H. (1974). The amount of hereditary disease in human populations. Ann. Hum. Genet. (Lond.) 38, 199–223.

UNSCEAR (1977). Report of the United Nations Scientific Committee on the Effects of Atomic Radiation. Sources and Effects of Ionizing Radiation. General Assembly Official Records, 32nd session, Suppl. 40, United Nations, New York.

UNSCEAR (1982). Report of the United Nations Scientific Committee on the Effects of Atomic Radiation. Ionizing Radiation: Sources and Biological Effects. General Assembly Official Records, 37th session, Suppl. 45, United Nations, New York.

UNSCEAR (1986). Report of the United Nations Scientific Committee on the Effects of Atomic Radiation. Genetic and Somatic Effects of Ionizing Radiation. General Assembly Official Records, 41st session, Suppl. 16, United Nations, New York.

UNSCEAR (1988). Report of the United Nations Scientific Committee on the Effects of Atomic Radiation. Sources, Effects and Risks of Ionizing Radiation. General Assembly Official Records, 43rd session, Suppl. 45, United Nations, New York.

Vizkelety T. (1986). Über Diagnostik der Stüftdysplasie. In: Kongenitale Dysplasien und Defekte des unsern Extremität, pp. 33–36 ( Chapchal G. , ed.). G. Thieme Verlag, Stuttgart.

Yoshimoto Y. Neel J. V. Schull W. J. Kato H. Soda M. Eto R. Mabuchi K. (1990). Malignant tumours during the first two decades of life in the offspring of atomic bomb survivors. Am. J. Hum. Genet. 46, 1041–1052.