Abstract
Most malignant neoplasms likely arise from the deleterious effects of environmental carcinogens. In addition, it appears that genetic predisposition or resistance governs responses of individuals to these agents. This interaction between environmental carcinogens and genetic factors has been termed ecogenetics. Ultimately, the final step in the genesis of malignant neoplasms involves molecular and/or cytogenetic alterations that free the cell from internal or external host regulatory control.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Ames B: Identifying environmental chemicals causing mutation and cancer. Science 204:587, 1979
Anderson DE: Genetic study of breast cancer: identification of a high risk group. Cancer 34:1090, 1974
Bader JL, Miller RW: Neurofibromatosis and childhood leukemia, J Pediatr 92:925, 1978
Barth RF, Khurana SK, Vergara GG, Lowman JT, Beckwith JB: Rapidly fatal familial histiocytosis associated with eosinophilia and primary immunological deficiency. Lancet 2:503, 1972
Berenblum I, Shubik P: A new quantitative approach to the study of stages of carcinogenesis in the mouse’s skin. Br J Cancer 1:383, 1947
Berger R, Bernheim A, Weh H-J, Flandria G, Daniel M-T, Brouet J-C, Colbert N: A new translocation in Burkitt tumor cells. Human Genet 53:111, 1979
Bernheim A, Berger R, Lenoir G: Cytogenetic studies on African Burkitt’s lymphoma cell lines: t(8;14), t(2;8) and t(8;22) translocations. Cancer Gen Cytogen 3:307, 1981
Blattner WA, Strober W, Muchmore AV, Blaese RM, Broder S, Fraumeni JF Jr: Familial chronic lymphocytic leukemia. Immunologic and cellular characterization. Ann Int Med 84:554, 1976
Boden G, Owen OE: Familial hyperglucagonemia: an autosomal dominant disorder. N Engl J Med 296:534, 1977
Bolande RP: Childhood tumors and their relationship to birth defects. In: Genetics of Human Cancer, J.J. Mulvihill, R.W. Miller, J.F. Fraumeni (eds). New York, Raven Press, pp. 43–75, 1977
Boveri T, Wurzburg C: Kabitzsch, Ueber mehrpolige Mitosen als Mittel zur Analyse des Zellkerns. Wurzburg, C. Kabitzsch, und Ver d phys med Ges zu Würzburg, NF Bd 35, 1902
Buehler SK, Firme F, Fodor G, Fraser GR, Marshall WH, Vaze P: Common variable immunodeficiency, Hodgkin’s disease, and other malignancies in a Newfoundland family. Lancet 1:195, 1975
Campbell WAB, Macafee AL, Wade WG: Familial neonatal leukemia, Arch Dis Child 37:93, 1962
Chaganti RSK: Significance of chromosome change to hematopoietic neoplasms, Blood 61:1269, 1983
Chitambar CR, Robinson WA, Glode LM: Familial leukemia and aplastic anemia associated with monosomy 7. Am J Med 75:756, 1983
Cohen AJ, Li FP, Berg S, Marchetto DJ, Tasi S, Jacobs SC, Brawn RS: Hereditary renal cell carcinoma associated with a chromosomal translocation. N Engl J Med 301:592, 1979
Cooper GM: Cellular transforming genes. Science 217:801, 1982
Croce CM, Shander M, Martinis J, Cicurel L, D’Ancona GG, Dolby ThW, Koprowski H: Chromosomal location of the genes for human immunoglobulin heavy chains. Proc Natl Acad Sci USA 76:3416, 1979
Dalla-Favera R, Bregni M, Erikson J, Patterson D, Gallo RC, Croce CM: Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. Proc Natl Acad Sci USA 79:7824, 1982
Delmas-Marsalet Y, Hors J, Colombani J, Dausett J: Study of HL-A genotypes in a case of familial chronic lymphocytic leukemia (CLL). Tissue Antigens 4:441, 1974
Donahue WL, Thompson MW: Familial lymphohistiocytosis. Birth Defects 8:105, 1972
Epstein CJ, Cox DR, Schonberg SA, Hogge WA: Recent developments in the prenatal diagnosis of genetic diseases and birth defects. Ann Rev Genet 17:49, 1983
Erikson J, Finan J, Nowell PC, Croce CM: Translocation of immunoglobulin VH genes in Burkitt lymphoma. Proc Natl Acad Sci USA 79:5611, 1982
Eriksson S, Hagerstrand I: Cirrhosis and malignant hematoma in alpha-1 antitrypsin deficiency. Acta Med Scand 195:451, 1974
Esseltine DW, DeLeeuw NKM, Berry GR: Malignant histiocytosis. Cancer 52:1904, 1983
Everson RB, Fraumeni JF Jr, Wilson RE, Norris HJ, Li FP, Fishman J, Stout D: Familial male breast cancer. Lancet 1:9, 1976
Farquhar JW, Claireaux AE: Familial haemophagocytic reticulosis. Arch Dis Child 27:519, 1952
Fraumeni JF, Rosen PJ, Hull EW, Barth RF, Shapiro SR, O’Connor JF: Hepatoblastoma in infant sister. Cancer 24:1086, 1969
Fraumeni JF Jr, Wetelecki W, Blattner WA, Jensen RD, Leventhal BG: Varied manifestations of a familial lympho-proliferative disorder. Am J Med 59:145, 1975
Frichot BC, Lynch HT, Guirgis HA, Harris RE, Lynch JF: New cutaneous phenotype in familial malignant melanoma. Lancet 1:864, 1977
Friedman-Birnbaum R, Abraham Z: Familial occurrence of Kaposi’s sarcoma. Report of two brothers. Tumori 69:365, 1983
Fudenberg HH: Are autoimmune diseases immunologic deficiency states? Hosp Pract 3:43, 1968
Fudenberg HH: Immunologic deficiency, autoimmune disease, and lymphoma: observations, implications, and speculations. Arthritis Rheum 9:464, 1966
Fudenberg HH: Are autoimmune diseases and malignancy due to selective T-cell deficiencies? In: Critical Factors in Cancer Immunology, J. Schultz, R.C. Leif (eds). New York, Academic Press, pp. 179–210, 1975
GeTaz EP, Staples WG: Familial Waldenström’s macro-globulinemia: case report. S Afr Med J 51:891, 1977
Gottlieb PD: Immunoglobulin genes. Molecular Immunol 17:1423, 1980
Greene MH, Miller RW: Familial non-Hodgkin’s lymphoma: histologic diversity and relation to other cancers. Am J Med Genet 1:437, 1978
Grufferman S, Cole P, Smith PG, Lukes RJ: Hodgkin’s disease in siblings. N Engl J Med 296:248, 1977
Hamasaki K: Chromosome abnormalities in Japanese Burkitt lymphoma cell lines. Acta Med Okayama 36:23, 1981
Hamilton LD: The Hiroshima and Nagasaki data and radiation carcinogenesis. Ann NY Acad Sci 114:241, 1964
Hanto DW, Frizzera G, Gajl-Peczalska KJ, Sakamoto K, Purtilo DT, Balfour HH, Simmons RL, NajarÃan JS: Epstein-Barr virus-induced B-cell lymphoma after renal transplantation: acyclovir therapy and transition from polyclonal to monoclonal B-cell proliferation. N Engl J Med 306:913, 1982
Harada S, Bechtold T, Seeley JK, Purtilo DT: Cell-mediated immunity to Epstein-Barr virus (EBV) and natural killer (NK)-cell activity in the X-linked lymphoproliferative syndrome. Int J Cancer 30:739, 1982
Heidelberger C: Chemical carcinogenesis. Annu Rev Biochem 44:79 (1975)
Higginson J: Present trends in cancer epidemiology. Proc Can Cancer Conf 8:40, 1969
Higginson J: The face of cancer worldwide. Hosp Practice 18:145, 1983
Jakobiec FA: Sebaceous adenoma of the eyelid and visceral malignancy. Am J Ophthalmol 78:952, 1974
Joncas JH, Rioux E, Wastiaux JP, Leyritz M, Robillard L, Menezes J: Nasopharyngeal carcinoma and Burkitt’s lymphoma in a Canadian family. I. HLA typing, EBV antibodies and serum immunoglobulins. Can Med Assoc J 115:858, 1976
Kantor AF, Blattner WA, Blot WJ, Fraumeni JF Jr, McLaughlin JK, Schuman LM, Lindquist LL, Wang N, Hozier JC: Hereditary renal carcinoma and chromosome defects. N Engl J Med 307:1403, 1983
Kersey JH, Spector BD, Good RA: Cancer in children with primary immunodeficiency diseases. J Pediatr 84:263, 1974
Kirsch IR, Morton CC, Nakahara K, Leder P: Human immunoglobulin heavy-chain genes map to a region of translocations in malignant B lymphocytes. Science 216:301, 1982
Klein G: Specific chromosome translocation and the genesis of B-cell-derived tumors in mice and men. Cell 32:311, 1983
Klein G: The role of gene dosage and genetic transpositions in carcinogenesis. Nature 294:313, 1981
Knudson AG, Strong LC: Mutation and cancer: neuroblastoma and pheochromocytoma. Am J Hum Genet 24:514, 1972
Knudson AG, Strong LC: Mutation and cancer: a model for Wilms’ tumor of the kidney. J Natl Cancer Inst 48:313, 1972
Kobayashi N, Furukawa T, Takatsu T: Congenital anomalies in children with malignancy. Paediatri Univ Tokyo 16:31, 1968
Kulkarni R, Netzloff ML, Texera C: Familial cryptorchidism and testicular tumors in non-twin brothers. Ann Clin Lab Science 13:327, 1983
Leder P, Battey J, Lenoir G, Moulding C, Murphy W, Potter H, Stewart T, Taub R: Translocation among antibody genes in human cancer. Science 222:765, 1983
Li FP, Fraumeni JF Jr: Soft-tissue sarcomas, breast cancer, and other neoplasms: a familial syndrome? Ann Intern Med 71:747, 1969
Li FP, Mcintosh S, Whang-Peng J: Double primary cancers in two young sibs, leukemia in another, and dextrocardia in a fourth. Cancer 39:2633, 1977
Li FP, Tucker MA, Fraumeni JF: Childhood cancer in sibs. J Pediatr 88:419, 1976
Lynch HJ, Frichot BC: Skin, heredity, and cancer. Semin Oncology 5:67, 1978
Lynch HT, Kaplan AR, Lynch JF: Klinefelter syndrome and cancer. A family study. J Am Med Assoc 229:809, 1974
Lynch HT, Mulcahy GM, Harris RE, Guirgis HA, Lynch JF: Genetic and pathologic findings in a kindred with hereditary sarcoma breast cancer, brain tumors, leukemia, lung, laryngeal, and adrenal cortical carcinoma. Cancer 41:2055, 1978
Lynch HT, Saldivar VA, Guirgis HA, Terasaki PI, Bardawil WA, Harris RE, Lynch JF, Thomas R: Familial Hodgkin’s disease and associated cancer. A clinical-pathologic study. Cancer 38:2033, 1976
MacMahon HE, Murphy AS, Bates MI: Endothelial-cell sarcoma of liver following thorotrast injections. Am J Pathol 23:585, 1947
Magrath I, Erikson J, Whang-Peng J, Sieverts H, Armstrong G, Benjamin D, Triche T, Alabaster O, Croce CM: Synthesis of kappa light chains by cell lines containing an 8;22 chromosomal translocation derived from a male homosexual with Burkitt’s lymphoma. Science 222:1094, 1983
Malcolm S, Barton P, Murphy C, Gerguson-Smith MA, Bentley DL, Rabbits TH: Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in-situ hybridization. Proc Natl Acad Sci USA 79:4957, 1982
Manolova Y, Manolov G, Kieler J, Levan A, Klein G: Genesis of the 14q+ marker in Burkitt’s lymphoma. Hereditas 90:5, 1979
Manolov G, Manolova Y, Levan A, Klein G: Experiments with fluorescent chromosome staining in Burkitt tumors. Hereditas 68:235, 1971
McBride OW, Hieter PA, Hollis GF, Swan D, Otey MD, Feder P: Chromosomal location of human kappa and lambda immunoglobulin light chain constant region genes. J Exp Med 155:1680, 1982
McKeen EA, Hanson MR, Mulvihill JJ, Glaubiger DL: Birth defects in Ewing’s sarcoma. N Engl J Med 309:1522, 1983
McKusick K: Mendelian Inheritance in Man. Baltimore, Johns Hopkins Press, pp. 1–1378, 1983
Meadows AT, Knudson AG: Regression of neuroblastoma IV-S: a genetic hypothesis. N Engl J Med 302:1254, 1980
Miller DR: Familial reticuloendotheliosis: concurrence of disease in five siblings. Pediatrics 38:986, 1966
Miller RW: Contrasting epidemiology of childhood osteosarcoma. Ewing’s tumor and rhabdomyosarcoma. Natl Cancer Inst Monogr 56:9, 1981
Miller RW: Cancer and congenital malformation: another view. In: Genetics of Human Cancer, J.J. Mulvihill, R.W. Miller, J.F. Fraumeni, Jr. (eds). New York, Raven Press, pp. 77–81, 1977
Miller RW, Fraumeni JF Jr, Hill JA: Neuroblastoma: epidemiologic approach to its origin. Am J Dis Child 115:253, 1968
Miyoshi I, Hiraki S, Kimura I, Miyamoto K, Sato J: 2/8 translocation in a Japanese Burkitt’s lymphoma. Experimentia 35:742, 1979
Mulvihill JJ: Genetic repertory of human neoplasia. In: Genetics of Human Cancer, J.J. Mulvihill, R.W. Miller, J.F. Fraumeni, Jr. (eds). New York, Raven Press, pp. 137–143, 1977
Mulvihill J, Gralnick H, Whang-Peng J, Leventhal B: Multiple childhood osteosarcomas in an American Indian family with erythroid macrocytosis and skeletal anomalies. Cancer 40:3115, 1977
Nicholson WJ: Cancer following occupational exposure to asbestos and vinyl chloride. Cancer 39:1792, 1977
Nowell PC, Hungerford DA: A minute chromosome in human chronic granulocytic leukemia. Science 132:1497, 1960
Ochs HD, Sullivan JL, Wedgwood RJ, Seeley JK, Sakamoto K, Purtilo DT: X-linked lymphoproliferative syndrome: abnormal antibody responses to bacteriophage 0X174. In: Primary Immunodeficiency Disease, R. Wedgwood, F. Rosen (eds). New York, Alan R. Liss, pp. 321–323, 1983
Omenn GS: Familial reticuloendotheliosis with eosinophilia. N Engl J Med 273:427, 1965
Petersen JM, Tubbs RR, Savage RA, Calabrese LC, Proffitt MR, Manolova Y, Manolov G, Shumaker A, Tatsumi E, McClain K, Purtilo DT: Small noncleaved B cell Burkitt-like lymphoma with chromosome t(8;14) translocation and carrying Epstein-Barr virus in a male homosexual with the acquired immune deficiency syndrome. Am J Med 78: 141, 1985
Potolsky AI, Heath CW, Buckley CE, Rowlands DT: Lymphoreticular malignancies and immunologic abnormalities in a sibship. Am J Med 50:42, 1971
Preussman R: Chemical carcinogens in human environment: problems and quantitative aspects. Oncology 33:51, 1976
Purtilo DT: Immune deficiency predisposing to Epstein-Barr virus-induced lymphoproliferative diseases: the X-linked lymphoproliferative syndrome as a model. In: Advances in Cancer Research, G. Klein, S. Weinhouse (eds). New York, Academic Press, pp. 379–312, 1980
Purtilo DT: Hypothesis: pathogenesis and phenotypes of an X-linked recessive lymphoproliferative syndrome. Lancet 2:882, 1976
Purtilo DT, Cassei CK, Yang JPS, Stephenson SR, Harper R, Landing BH, Vawter GF: X-linked recessive progressive combined variable immunodeficiency (Duncan’s disease). Lancet 1:935, 1975
Purtilo DT, Cohen S: Diet, nutrition and cancer. Postgraduate Medicini 78: 193, 1985
Purtilo DT, DeFlorio D, Hutt LM, Bhawan J, Yang JPS, Otto R, Edwards W; Variable phenotypic expression of an X-linked recessive lymphoproliferative syndrome. N Engl J Med 297:1077, 1977
Purtilo DT, Liao SA, Sakamoto K, Snyder LM, DeFlorio D, Bhawan J, Paquin LA, Yang JPS, Hutt-Fletcher LM, Muralidharan K, Raff P, Saemundsen AK, Klein G: Diverse familial malignant tumors and Epstein-Barr virus. Cancer Res 41:4248, 1981
Purtilo DT, Paquin L, Gindhart G: Genetics of neoplasia — Impact of ecogenetics on oncogenesis. Am J Pathol 91:609, 1978
Purtilo DT, Paquin LA, DeFlorio D, Virzi F, Sikhuja R: Immunodiagnosis and immunopathogenesis of the X-linked recessive lymphoproliferative syndrome. Sem Hematol 16:309, 1979
Purtilo DT, Riordan JA, DeFlorio D, Yang JPS, Sun P, Vawter G: Immunological disorders and malignancies in five young brothers. Arch Dis Child 52:310, 1977
Purtilo DT, Sakamoto K, Barnabei V, Seeley J, Bechtold T, Rogers G, Yetz J, Harada S: Epstein-Barr virus-induced diseases in males with the X-linked lymphoproliferative syndrome (XLP). Am J Med 73:49, 1982
Purtilo DT, Yang JPS, Allegra S, DeFlorio D, Hutt LM, Soltani M, Vawter G: Hematopathology and pathogenesis of the X-linked recessive lymphoproliferative syndrome. Am J Med 62:225, 1977
Purtilo DT, Yang JPS, Cassei CK, Harper P, Stephenson SR, Landing BH, Vawter GF: X-linked recessive progressive combined variable immunodeficiency (Duncan’s disease). Lancet 1:935, 1975
Rapp F, Reed CL: The viral etiology of cancer: a realistic approach. Cancer 40:419, 1977
Razis DV, Diamond HD, Cravar LF: Familial Hodgkin’s disease: its significance and implications. Ann Inter Med 51:933, 1959
Reich SD, Wiernik PH: Von Recklinghausen neurofibromatosis and acute leukemia. Am J Dis Child 130:888, 1976
Rosen NA, Gergely P, Yando M, Klein G, Britton S: Polyclonal Ig production after Epstein-Barr virus infection of human lymphocytes in vitro. Nature 267:52, 1977
Rosen PP, Lyngholm B, Kinne DW, Eattie EJ: Juvenile papillomatosis of the breast and family history of breast carcinoma. Cancer 49:2591, 1982
Sakamoto K, Freed H, Purtilo DT: Antibody response to Epstein-Barr virus in families with the X-linked lympho-proliferative syndrome. J Immunol 125:921, 1980
Sandberg AA, Wake N: Chromosomal changes in primary and metastatic tumors and in lymphoma. In: Genes, Chromosomes, and Neoplasia, F.E. Arrighi, P.N. Rao, E. Stubblefield (eds). New York, Raven Press, pp. 297–333, 1981
Sanger W, Howe J, Fordyce R, Purtilo DT: Inherited partial trisomy 15 complicated by neuroblastoma. Cancer Genet Cytogenet 11:253, 1984
Sarrazin R, Dyon J, Boat M, Rossignol A, Rachail M, Fournet J, Faure H: Le syndrome de Zollinger-Ellison chez l’enfant. Reflexions a propos d’un cas et revue de la literature. Ann Pediatr 24:863, 1977
Scheike O: Male breast cancer. Acta Pathol Microbiol Scand 251:13, 1975
Scheike O, Visfeldt J, Patersen B: Male breast cancer. III. Breast carcinoma in association with the Klinefelter syndrome. Acta Pathol Microbiol Scand 81:352, 1973
Schweich L: Cheilitis glandularis simplex. Arch Dermtol 89:301, 1964
Seeley JK, Bechtold T, Purtilo DT, Lindsten T: NK deficiency in X-linked lymphoproliferative syndrome. In: Natural Killer Cells and Other Natural Effector Cells, R.B. Herberman (ed). New York, Academic Press, Vol. 2, pp. 1211–1218, 1982
Seeley JK, Sakamoto K, Ip S, Hansen P, Purtilo DT: Abnormal subsets in the X-linked lymphoproliferative syndrome. J Immunol 127:2618, 1981
Seeley JK, Harada S, Bechtold T, Ochs H, Wedgwood RJ, Sakamoto K, Lindsten T, Yetz J, Purtilo DT: Primary and acquired immune defects in X-linked lymphoproliferative syndrome (XLP), Submitted for publication.
Shandler M, Martinis J, Croce CM: Genetics of human immunoglobulins: assignment of the genes for mu, alpha, and gamma immunoglobulin chains to human chromosome 14. Transplant Proc 12:417, 1980
Sheng-Ong GLC, Keath EJ, Piccoli SP, Cole MD: Novel myc oncogene RNA from abortive immunoglobulin-gene recombination in mouse plasmacytomas. Cell 31:443, 1982
Snyder AL, Henderson ES, Li FP, Todaro GJ: Possible inherited leukemogenic factors in familial acute myelogenous leukemia. Lancet 1:586, 1970
Sorenson SA, Jensen OA, Klinken L: Familial aggregation of neuroectodermal and gastrointestinal tumors. Cancer 52:1977, 1983
Stivrins TJ, Davis RB, Sanger W, Fritz J, Purtilo DT: Transformation of Fanconi’s anemia to acute non-lymphocytic leukemia associated with emergence of monosomy 7. Blood 64: 173, 1984
Taub R, Kirsch I, Morton C, Lenoir G, Swan D, Tronick S, Aaronson S, Leder P: Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells. Proc Natl Acad Sci USA 79:7837, 1982
Temin HM: The protovirus hypothesis. J Natl Cancer Inst 46:3, 1971
Till MM, Jones LH, Pentycross CR, Hardisty RM, Lawler SD, Harvey GAM, Soothill JF: Leukemia in children and their grandparents: studies of immune function in six families. Br J Haematol 29:575, 1975
Trage KH, Mayre WR: Familial islet-cell adenomatosis. Lancet 2:426, 1977
Tyzzer EE: A study of heredity in relation to the development of tumors in mice. J Med Res 17:199, 1907
Van Den Berghe H, Parloir C, Gosseye S, Englebieme V, Cornu G, Sokal G: Variant translocation in Burkitt lymphoma. Cancer Genet Cytogenet 1:9, 1979
Weber W, Ott J, Gencik A, Muller HJ: Familial cancer: genetically determined? Anticancer Research 3:133, 1982
Wennstrom J, Pierce ER, McKusik VA: Hereditary benign and malignant lesions of the large bowel. Cancer 34:850, 1974
Westin EH, Wong-Staal F, Gelmann EP, Dalla-Favera R, Papas TS, Lautenberger JA, Eva A, Reddy EP, Tronich SR, Aaronson SA, Gallo RC: Expression of cellular homologues of retroviral onc genes in human hematopoietic cells. Proc Natl Acad Sci USA 79:4290, 1981
Wynder EL, Gori GB: Contribution of the environment to cancer incidence: an epidemiologic exercise. J Natl Cancer Inst 58:825, 1977
Youinou P, LeGoff P, Saleun JP, Fauchier C, LeMenn G: Les gammapathies monoclonales familiales. Sem Hop Paris 53:1367, 1977
Yunis JJ: Chromosomes and cancer: new nomenclature and future directions. Human Pathol 12:494, 1981
Yunis JJ: The chromosomal basis of human neoplasia. Science 221:227, 1983
Ziegler JL, Magrath IT, Gerber P, Levine PH: Epstein-Barr virus and human malignancy. Ann Intern Med 86:323, 1977
Updated reference
Purtilo DT, Geelhoed GW, Li FP, et al.: Mucinous colon carcinoma in a black family. Cancer Gemet Cytogenet 24:11, 1987
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1989 Kluwer Academic Publishers, Dordrecht
About this chapter
Cite this chapter
Purtilo, D.T., Linder, J., Manolov, G., Manolova, Y. (1989). Genetic Diseases, Hamartomas, and Familial Occurrence of Neoplasms. In: Levine, A.S. (eds) Etiology of Cancer in Man. Cancer Growth and Progression, vol 6. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-2532-8_3
Download citation
DOI: https://doi.org/10.1007/978-94-009-2532-8_3
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-010-7644-9
Online ISBN: 978-94-009-2532-8
eBook Packages: Springer Book Archive