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References General References (Chapter 1) References General References (Chapter 1) Asimov, I. 1962. The genetic code. New Amer. Libr. World Lit., Inc., New York. Baltzer, F. 1962. Theodor Boveri. Leben und Werk eines grossen Biologen. 1862-1915. Wissensch. VerI. Gesellsch. m. b. H., Stuttgart. Brown, W. V. 1972. Textbook of cytogenetics. C. V. Mosby Co., Saint Louis, MO. Cohn, N. S. 1969. Elements of cytology. 2nd ed. Harcourt, Brace and World, Inc., New York, N. Y. Dampier, W. C. 1943. A history of science and its relations with philosophy and religion. Cambridge Univ. Press, Cambridge. Darlington, C. D. 1964. Genetics and man. Schocken Books, New York. Dawes, B. 1952. A hundred years of biology. Duckworth and Co., London. De Beer, G. 1964. Charles Darwin. Doubleday, New York. Dunn, L. C. (ed.) 1951. Genetics in the 20th century. Macmillan, New York. Gabriel, M. L., and S. Fogel (eds.) 1955. Great experiments in biology. Prentice-Hall, Inc., Englewood Cliffs, N. J. Gardner, E. J. 1960. Principles of genetics. John Wiley and Sons, Inc., New York. Glass, B., O. Temkin and W. L. Strauss, Jr. 1959. Forerunners of Darwin, 1745-1859. Johns Hopkins Press, Baltimore. Goldschmidt, R. B. 1956. Portraits from memory. Univ. Washington Press, Seattle. Goldschmidt, R. B. 1960. In and out of the ivory tower; the autobiography of Richard B. Goldschmidt. Univ. Wash. Press, Seattle. Hamerton, J. L. 1971. Human cytogenetics. Vol. I and II. Academic Press, New York, N.Y. Hughes, A. 1959. A history of cytology. Abelard-Schuman, New York. Jaffe, B. 1944. Men of science in America; the role of science in the growth of our coun­ try. Simon and Schuster, New York. King, R. C. 1968. A dictionary of genetics. Oxford Univ. Press, New York, N. Y. Nordenski5ld, E. 1935. The history of biology. A survey. Tudor Publishing Co., New York. Rieger, R. A. Michaelis and M. M. Green. 1968. A glossary of genetics and cytogenetics, classical and molecular. 3rd ed. Springer-Verlag New York Inc. Schrader, F. 1948. Three quarter-centuries of cytology. Science 107: 155-159. Stern, C. 1968. Genetic mosaics, and other essays. Harvard Univ. Press, Cambridge. Stubbe, H. 1972. History of genetics. Massachusetts Inst. Tech. Press, Cambridge, Mass. Swanson, C. P. 1957. Cytology and cytogenetics. Prentice-Hall, Inc., Englewood Cliffs, N.J. Taylor, G. R. 1963. The science of life. A picture history of biology. McGraw-Hill Book Co., Inc., New York, N. Y. Wilson, E. B. 1925. The cell in development and heredity. 3rd ed. Macmillan Co., New York, N. Y. Specific References Abbe, E. 1886. Sitzber. Jen. Gesell. Med. Naturwiss. 1886:107. Abo EI-Nil, M. M., and A. C. Hildebrandt. 1973. Origin of androgenetic callus and hap­ loid geranium plants. Can. J. Bot. 51:2107-2109. Absate, M., and D. S. Borgaonkar. 1977. Chromosome arm involvement in interchanges. Lancet 1:96. Ahloawalia, B. S. 1969. Desynapsis in diploid and tetraploid clones of ryegrass. Genetica 40:379-392. Al Aish, M. S., F. de la Cruz, A. Goldsmith, J. Volpe, G. Mella, and J. C. Robinson. 1967. Autosomal monosomy in man. Complete monosomy G(21-22) in a four-and­ one-half-year-old mentally retarded girl. New Engl. J. Med. 277:777-784. Albers, F. 1972. Cytotaxonomie und B-Chromosomen bei Deschampsia caespitosa (L.) P.B. und verwandten Arten. Beitr. BioI. Pflanz. 48:1-62. Alexander, G. 1954. Biology. 7th ed. Barnes and Noble, New York. Alexander, M. L. 1952. The effect of two pericentric inversions upon crossing over in Drosophila melanogaster. Univ. Texas Publ. 5204:219-226. Alfert, M., and I. I. Geschwindt. 1958. The development of polysomaty in rat liver. Exptl. Cell Res. 15:230-235. Alii, O. S., G. N. Donnell, B. F. Crandall et al. 1973. Deletion of the short arm of chro­ mosome 9(46,9p-): A new deletion syndrome. Ann. Genet. (Paris) 16:17. Alii, o. S., R. G. Sanger, A. E. Sweeny, and G. N. Donell. 1974.46 del(9)(22:): A new deletion syndrome. In: Bergsma, D. (ed.). Clinical cytogenetics and genetics. Birth Defects: Orig. Art. Ser. 10:27-35. Allard, R. W. 1953. A gene in lima beans pleiotropically affecting male-sterility and seedling abnormality. Proc. Amer. Soc. Hort. Sci. 61:467-471. Allderdice, P. W., N. Browne, and D. P. Murphy. 1975. Chromosome 3 duplication q21---+qter deletion p25---+pter syndrome in children of carriers of a pericentric inversion inv (3)(p25q21). Amer. J. Human Genet. 27:699-718. Allderdice, P. W., J. G. Davis, O. J. Miller, H. P. Klinger, D. Warburton, D. A. Miller, F. H. Allen, Jr., C. A. L. Abrams, and E. McGilvray. 1969. The 13q- deletion syn­ drome. Amer. J. Hum. Genet. 21:499-512. Allderdice, P. W., O. J. Miller, P. L. Pearson, G. Klein, and H. Harris. 1973. Human chromosomes in 18 men-mouse somatic cell lines analyzed by quinacrine fluorescence. J. Cell. Sci. 12:809-830. Allderdice, P. W. and T. A. Tedesco. 1975. Localization of the human gene for galactose­ I-phosphate uridyltransferase to 3q21---+qter by quantitative enzyme assay. Lancet 1975-11:39. Allderdice, P. W., W. D. Heneghan and E. T. Felismino. 1976. 9pter---+p22 deletion syn­ drome: A case report. Birth Defects: Orig. Art. Ser. 13:151-155. Allen, N. S., G. B. Willson, and S. Powell. 1950. Comparative effects of colchicine and sodium nucleate. J. Hered. 41: 159-163. 350 References AI-Yasari, S. 1967. Studies of toluidine blue for inducing haploidy in Lycopersicon escu­ lentum and Zea mays. Ph.D. Thesis, Univ. New Hampshire. AI-Yasari, S. and O. Rogers. 1971. Attempting chemical induction of haploidy using toluidine blue. J. Am. Soc. Hort. Sci. 96:126-127. Ames, B. N., and P. E. Hartman. 1963. The histidine operon. Cold Spring Harbor Symp. Quant. BioI. 28:349-356. Anders, G., A. Prader, E. Hauschteck, K. Schlirer, R. E. Siebenmann and R. Heller. 1960. Multiple Sex-Chromatin und komplexes chromosomales Mosaik bei einem Kna­ ben mit Idiotie und multiplen Misbildungen. Helv. Paediat. Acta 15:515-532. Anders, J. M., G. M. Jagiello, P. E. Polani, F. Gianelli, J. L. Hamerton, and D. M. Leiberman. 1968. Chromosome findings in chronic psychotic patients. Brit. J. Psychiat. 114:1167-1174. Anderson, E. 1947. A case of asyndesis in Picea abies. Hereditas 33:301-347. Anderson, E., and K. Sax. 1936. A cytological monograph of the American species of Tradescantia. Bot. Gaz. 97:433-476. Anderson, E. 1968. Oocyte differentiation in the sea urchin Arbacia punctulata. with particular reference to the origin of cortica granules and their participation in the cor­ tical reaction. J. Cell BioI. 37:514-539. Anderson, E. G. 1943. Utilization of translocations with endosperm markers in the study of economic traits. Use of translocations in corn breeding. Maize Genet. Coop. News­ letter 17:4-5. Anderson, E. G. 1956. The application of chromosomal techniques to maize improve­ ment. Brookhaven Symp. BioI. 9:23-36. Arber, W. 1958. Transduction characteres Gal par Ie bacteriophage lambda. Arch. Sci. (Geneva) 11:259-338. Archebald, E. E. A. 1939. The development of the ovule and seed of jointed cactus (Opuntia aurantiaca Lindley). South Afric. J. Sci. 36:195-211. Asay, K. H. 1977. Forage and range program. Logan, Utah. 24th Grass Breed. Work Plann. Conf., Tifton, Georgia, p. 35. Asker, S. 1976. Apomixis and sexuality in diploid and trisomic Potentilla argentea A. Hereditas 83:35-38. Atanasoff, D. 1964a. Viruses and cytoplasmic heredity. Z. Pflanzenz. 51:197-214. Atanasoff, D. 1964b. Phytopathol. Z. 50:336-358. Aula, P. 1963. Chromosome breaks in leucocytes of chicken pox patients. Preliminary communication. Hereditas 49:451-453. Aula, P., U. Gripenberg, L. Hjelt, E. Kivalo, J. Leisti, J. Palo, B. von Schoultz, and E. Suomalainen. 1967. Two cases with a ring chromosome in group E. Acta Neurol. Scan­ dinav.43 (suppl. 31):51-52. Austin, C. R. 1969. Fertilization and development of the egg. In: Cole, H. H. and P. T. Cupps. (eds.) Reproduction in domestic animals. Academic Press, New York, pp. 355- 384. Avanzi, S., P. G. Cionini, and F. D'Amato. 1970. Cytochemical and autoradiographic analyses on the embryo suspensor cells of Phaseolus coccineus. Caryologia 23:605-638. Avery, A. G., S. Satina, and J. Rietsema. 1959. Blakeslee: The genus Datura. Ronald Press, Co., New York. Avery, O. T., C. M. MacLeod, and M. McCarty. 1944. Studies on the chemical nature of the substance inducing transformation of pneumococcal types. Induction of trans­ formation by a desoxyribonuc1eic acid fraction isolated from Pneumococcus type III. J. Exp. Med. 79:137-158. Azael, A. 1973. Beitrlige zur Aufstellung eines Trisomen-Sortiments beim Hafer, Avena sativa L. Z. Pflanzenz. 70:289-305. Babcock, E. B., and G. L. Stebbins. 1938. The American species of Crepis. Publ. Car­ negie Inst. Wash. 504:1-199. Badenhuizen, N. P. 1941. Experimentally produced haploids in Nicotiana tabacum by means of x-rays. Natourewetensch. Tijdf. Nederl.-Indie. 101:240-242. Baer, K. E. von. 1827. De ovi mamalium et hominis genesi. Leipzig. References 351 Baer, K. E. von. 1828. tiber die Entwicklungsgeschichte der Tiere. K5nigsberg. Baglioni, C. 1962. The fusion of two peptide chains in hemoglobin Lepore and its inter­ pretation as a genetic deletion. Proc. Natl. Acad. Sci. U.S.A. 48:1880-1886. Baikie, A. G., W. M. Court Brown, K. E. Buckton, D. G. Harnden, P. A. Jacobs, and I. M. Tough. 1960. A possible specific chromosome abnormality in human chronic mye­ loid leukemia. Nature 188:1165-1166. Bajer, A. 1965. Subchromatid structure of chromosomes in the living state. Chromosoma 17:291-302. Bajer, A., and J. Mole-Bajer. 1954. Acta Soc. Botan. Polon. 23:69. Cited in: Mazia, D. 1961. Bajer, A., and J.
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