12. G E N E T I C C Y T O L O G Y
453
Delhanty, J. D . A . , Ellis, J. R . and R o w l e y , P. T . (1961). Triploid cells in a human
embryo. Lancet (i), 1286.
Demerec, M . (1939). T h e nature o f changes in the white-notch region o f the X -
chromosome o f Drosophila melanogaster. "Proceedings o f the 7th International
Congress o f Genetics", p . 99.
Demerec, M . and Slizynska, H . (1937). Mottled white 258-18 o f Drosophila melanogaster. Genetics 22, 641.
Dewey, W . C . and Humphrey, R . M . (1962). Relative radiosensitivity o f different
phases in the life cycle o f L-P59 mouse fibroblasts and ascites tumor cells.
Radiat. Res. 16, 503.
Djordjevic, B. and Szybalski, W . (1960). Genetics o f human cell lines. I I I . Incorporation o f 5-bromo- and 5-iododeoxyuridine into the deoxyribonucleic acid of
human cells and its effect on radiation sensitivity. J. exp. Med. 112, 509.
Doniach, I. and Pelc, S. R . (1950). Autoradiograph technique. Brit. J. Radiol. 23, 184.
Drew, R . M . and Painter, R . B. (1959). Action o f tritiated thymidine on the clonal
growth o f mammalian cells. Radiat. Res. 11, 535.
D u n n , D . B. and Smith, J. D . (1954). Incorporation o f halogenated pyrimidines into
the deoxyribonucleic acids o f Bacterium coli and its bacteriophages. Nature, Lond.
174, 305.
Editorial (1959a). T h e chromosomes o f man. Lancet (i), 715.
Editorial (1959b). H u m a n chromosomal abnormalities. Lancet (ii), 448.
Edwards, J. H . (1960). Painless skin biopsy. Lancet (i), 496.
Edwards, J. H . , Harnden, D . G., Cameron, A . H . , Crosse, V . M . and Wolff, O . H .
(1960). A new trisomic syndrome. Lancet (i), 787.
Edwards, J. L. and Klein, R . E. (1961). Cell renewal in adult mouse tissues. Amer. J.
Path. 38, 437.
Edwards, J. L., K o c h , A . L., Youcis, P., Freese, H . L., Laite, M . B. and Donalson,
J. T . (1960). Some characteristics o f D N A synthesis and the mitotic cycle in
Ehrlich ascites tumor cells. J. biophys. biochem. Cytol. 7, 273.
Edwards, J. H . and Y o u n g , R . B. (1961). Chromosome analysis from small volumes
of blood. Lancet (ii), 48.
Ferguson-Smith, M . A . (1961). Chromosomes and human disease. In "Progress in
Medical Genetics" (A. G. Steinberg, e d . ) , p . 292. Grune and Stratton, N e w York.
Ferguson-Smith, M . A . and Handmaker, S. C . (1961). Observations on the satellited
human chromosomes. Lancet (i), 638.
Ferguson-Smith, M . A . , Johnston, A . W . and Handmaker, S. D . (1960a). Primary
amentia and micro-orchidism associated with X X X Y sex-chromosome constitution. Lancet (ii), 184.
Ferguson-Smith, M . A . , Johnston, A . W . and Weinberg, A . N . (1960b). T h e
chromosome complement in true hermaphroditism. Lancet (ii), 126.
Ficq, A . and Pavan, C. (1957). Autoradiography o f polytene chromosomes o f
Rhynchosciara angelae at different stages o f larval development. Nature, Lond. 180,
983.
Fitzgerald, P. J., Eidinoff, M . L., Knoll, J. E. and Simmel, E. B. (1951). Tritium in
autoradiography. Science 114, 494.
Ford, C. E. (1960). H u m a n cytogenetics: Its present place and future possibilities.
Amer. J. hum. Genet. 12, 104.
Ford, C. E. and Hamerton, J. L. (1956). T h e chromosomes o f man. Nature, Lond. 178,
1020.
Ford, C. E., Jacobs, P. A . and Lajtha, L. G. (1958). H u m a n somatic chromosomes.
Nature, Lond. 181, 1565.
Précédent

- 460/791

Suivant