4 5 4
T . G . HSU
Ford, C . E., Jones, K . W . , Miller, O . J., M i t t w o c h , U . , Penrose, L. S., Ridler, M .
and Shapiro, A . (1959a). T h e chromosomes in a patient showing both mongolism
and the Klinefelter syndrome. Lancet (i), 709.
Ford, C . E., Jones, K . W . , Polani, P. E., Almeida, J. G. de and Briggs, J. H . (1959b).
A sex-chromosome anomaly in a case o f gonadal dysgenesis (Turner's syndrome).
Lancet (i), 711.
Ford, C . E., Polani, P. G . , Briggs, J. H . and Bishop, P. M . F. (1959c). A presumptive
human X X Y / X X mosaic. Nature, Lond. 183, 1030.
Fraccaro, M . , Kaijser, K . and Lindsten, J. (1959). C h r o m o s o m e complement in
gonadal dysgenesis (Turner's syndrome). Lancet (i), 886.
Fraccaro, M . , Kaijser, K . and Lindsten, J. (1960a). Chromosomal abnormalities in
father and m o n g o l child. Lancet (i), 724.
Fraccaro, M . , Kaijser, K . and Lindsten, J. (1960b). A child with 49 chromosomes.
Lancet (ii), 899.
Fraser, J. H . , Campbell, J., MacGillivray, R . C , Boyd, E. and Lennox, B. (1960).
T h e X X X syndrome: Frequency a m o n g mental defectives and fertility. Lancet
(ii), 626.
Freese, E., Bautz-Freese, E. and Bautz, E. (1961). Hydroxylamine as a mutagenic
and inactivating agent. J. mol. Biol. 3, 133.
Friedkin, M . , Tilson, D . and Roberts, D . (1956). Studies o f deoxyribonucleic acid and
biosynthesis in embryonic tissues with t h y m i d i n e - C
1 4
. J. biol. Chem. 220, 627.
Gall, J. G . (1959). Macronuclear duplication in the ciliated protozoan Euplotes.
J. biophys. biochem. Cytol. 5, 295.
Gelfant, S. (1962). Initiation o f mitosis in relation to the cell division cycle. Exp. Cell
Res. 26, 395.
Gey, G . O . , Bang, F. B. and Gey, M . K . (1954). Responses o f a variety o f normal and
malignant cells to continuous cultivation, and some practical applications o f
these responses to problems in the biology o f disease. Ann. N.T. Acad. Sci. 58, 976.
D e Grouchy, J., L a m y , M . , Frezal, J. and Ribier, J. (1961). X X / X O mosaics in
Turner's syndrome. Lancet (i), 1369.
G r u m b a c h , M . M . and Morishima, A . (1962). Sex chromatin and the sex c h r o m o -
somes: O n the origin o f sex chromatin from a single X c h r o m o s o m e . Acta cytol.
6, 46.
Hamerton, J. L., Cowie, V . A . , Giannelli, F., Briggs, S. M . and Polani, P. E. (1961).
Differential transmission o f D o w n ' s syndrome (mongolism) through male and
female translocation carriers. Lancet (ii), 956.
Hannah, A . (1951). Localization and function o f heterochromatin in Drosophila
melanogaster. Advanc. Genet. 4, 87.
Harnden, D . G . (1960a). T h e chromosomes. In " R e c e n t Advances in H u m a n
Genetics" (L. S. Penrose, e d . ) , p . 19. Churchill, L o n d o n .
Harnden, D . G . (1960b). A human skin culture technique used for cytological
examination. Brit. J. exp. Path. 41, 31.
Harnden, D . G . and Armstrong, C . N . (1959). T h e chromosomes o f a true hermaphrodite. Brit. med. J. 2, 1287.
Hayflick, L. and M o o r h e a d , P. S. (1961). T h e serial cultivation o f human diploid cell
strains. Exp. Cell Res. 25, 585.
Hayward, M . D . (1960). Sex chromosome mosaicism in man. Heredity 15, 235.
Hayward, M . D . and Bower, B. D . (1960). Chromosomal trisomy associated with the
Sturge-Weber syndrome. Lancet (ii), 844.
Heitz, E. (1933). Die somatische Heteropyknose bei Drosophila melanogaster und ihre
genetische Bedeutung. Z- Z
e
W
orsca
-
20, 237.
T . G . HSU
Ford, C . E., Jones, K . W . , Miller, O . J., M i t t w o c h , U . , Penrose, L. S., Ridler, M .
and Shapiro, A . (1959a). T h e chromosomes in a patient showing both mongolism
and the Klinefelter syndrome. Lancet (i), 709.
Ford, C . E., Jones, K . W . , Polani, P. E., Almeida, J. G. de and Briggs, J. H . (1959b).
A sex-chromosome anomaly in a case o f gonadal dysgenesis (Turner's syndrome).
Lancet (i), 711.
Ford, C . E., Polani, P. G . , Briggs, J. H . and Bishop, P. M . F. (1959c). A presumptive
human X X Y / X X mosaic. Nature, Lond. 183, 1030.
Fraccaro, M . , Kaijser, K . and Lindsten, J. (1959). C h r o m o s o m e complement in
gonadal dysgenesis (Turner's syndrome). Lancet (i), 886.
Fraccaro, M . , Kaijser, K . and Lindsten, J. (1960a). Chromosomal abnormalities in
father and m o n g o l child. Lancet (i), 724.
Fraccaro, M . , Kaijser, K . and Lindsten, J. (1960b). A child with 49 chromosomes.
Lancet (ii), 899.
Fraser, J. H . , Campbell, J., MacGillivray, R . C , Boyd, E. and Lennox, B. (1960).
T h e X X X syndrome: Frequency a m o n g mental defectives and fertility. Lancet
(ii), 626.
Freese, E., Bautz-Freese, E. and Bautz, E. (1961). Hydroxylamine as a mutagenic
and inactivating agent. J. mol. Biol. 3, 133.
Friedkin, M . , Tilson, D . and Roberts, D . (1956). Studies o f deoxyribonucleic acid and
biosynthesis in embryonic tissues with t h y m i d i n e - C
1 4
. J. biol. Chem. 220, 627.
Gall, J. G . (1959). Macronuclear duplication in the ciliated protozoan Euplotes.
J. biophys. biochem. Cytol. 5, 295.
Gelfant, S. (1962). Initiation o f mitosis in relation to the cell division cycle. Exp. Cell
Res. 26, 395.
Gey, G . O . , Bang, F. B. and Gey, M . K . (1954). Responses o f a variety o f normal and
malignant cells to continuous cultivation, and some practical applications o f
these responses to problems in the biology o f disease. Ann. N.T. Acad. Sci. 58, 976.
D e Grouchy, J., L a m y , M . , Frezal, J. and Ribier, J. (1961). X X / X O mosaics in
Turner's syndrome. Lancet (i), 1369.
G r u m b a c h , M . M . and Morishima, A . (1962). Sex chromatin and the sex c h r o m o -
somes: O n the origin o f sex chromatin from a single X c h r o m o s o m e . Acta cytol.
6, 46.
Hamerton, J. L., Cowie, V . A . , Giannelli, F., Briggs, S. M . and Polani, P. E. (1961).
Differential transmission o f D o w n ' s syndrome (mongolism) through male and
female translocation carriers. Lancet (ii), 956.
Hannah, A . (1951). Localization and function o f heterochromatin in Drosophila
melanogaster. Advanc. Genet. 4, 87.
Harnden, D . G . (1960a). T h e chromosomes. In " R e c e n t Advances in H u m a n
Genetics" (L. S. Penrose, e d . ) , p . 19. Churchill, L o n d o n .
Harnden, D . G . (1960b). A human skin culture technique used for cytological
examination. Brit. J. exp. Path. 41, 31.
Harnden, D . G . and Armstrong, C . N . (1959). T h e chromosomes o f a true hermaphrodite. Brit. med. J. 2, 1287.
Hayflick, L. and M o o r h e a d , P. S. (1961). T h e serial cultivation o f human diploid cell
strains. Exp. Cell Res. 25, 585.
Hayward, M . D . (1960). Sex chromosome mosaicism in man. Heredity 15, 235.
Hayward, M . D . and Bower, B. D . (1960). Chromosomal trisomy associated with the
Sturge-Weber syndrome. Lancet (ii), 844.
Heitz, E. (1933). Die somatische Heteropyknose bei Drosophila melanogaster und ihre
genetische Bedeutung. Z- Z
e
W
orsca
-
20, 237.