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• W1994579911 abstract "HereditasVolume 55, Issue 1 p. 55-67 Open Access CHROMOSOME DNA SYNTHESIS IN THE CELLS OF A HUMAN TRIPLOID/DIPLOID MOSAIC LEONARD ATKINS, LEONARD ATKINS INSTITUTE FOR MEDICAL GENETICS, UPPSALA, SWEDEN Massachusetts General Hospital, Boston, Massachusetts, 02114, U.S.A.Search for more papers by this authorJ. A. BÖÖK, J. A. BÖÖK INSTITUTE FOR MEDICAL GENETICS, UPPSALA, SWEDENSearch for more papers by this authorBERTA SANTESSON, BERTA SANTESSON INSTITUTE FOR MEDICAL GENETICS, UPPSALA, SWEDENSearch for more papers by this author LEONARD ATKINS, LEONARD ATKINS INSTITUTE FOR MEDICAL GENETICS, UPPSALA, SWEDEN Massachusetts General Hospital, Boston, Massachusetts, 02114, U.S.A.Search for more papers by this authorJ. A. BÖÖK, J. A. BÖÖK INSTITUTE FOR MEDICAL GENETICS, UPPSALA, SWEDENSearch for more papers by this authorBERTA SANTESSON, BERTA SANTESSON INSTITUTE FOR MEDICAL GENETICS, UPPSALA, SWEDENSearch for more papers by this author First published: August 1966 https://doi.org/10.1111/j.1601-5223.1966.tb02035.xCitations: 2 AboutPDF ToolsExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Literature cited Atkins, L., Gustavson, K.-H. and Hansson, O. 1963. A case of XXXXY sex chromosome anomaly with autoradiographic studies. Cytogenetics 2: 208– 232. Atkins, L. and Santesson, Berta. Chromosome DNA synthesis in cultured normal human female skin cells. Hereditas 55: 39– 46. Böök, J. A., Atkins, L. and Santesson, Berta 1963. Some new data on autosomal aberrations in man. Path. Biol. 11: 1159– 1162. Böök, J. A., Masterson, J. B. and Santesson, Berta 1962. Malformation syndrome associated with triploidy—further chromosome studies of the patient and his family. Acta Genet. 12: 193– 201. Böök, J. A. and Santesson, Berta 1960. Malformation syndrome in man associated with triploidy (69 chromosomes). Lancet i: 858– 859. Böök, J. A. and Santesson, Berta 1961. Nuclear sex in triploid XXY human cells. Lancet ii: 318. Böök, J. A., Santesson, Berta and Zetterqvist, P. 1961. Association between congenital heart malformation and chromosomal variations. Acta Paediat. Sthlm. 50: 217– 227. Carr, D. H. 1963. Chromosome studies in abortuses and stillborn infants. Lancet ii: 603– 606. Ferrier, P., Ferrier, S., Stalder G., BÜhxer, E., Bamatter, F. and Klein, D. 1964. Congenital asymmetry associated with diploid-triploid mosaicism and large satellites. Lancet i: 80– 82. German, J. 1963. The pattern of DNA synthesis in the chromosomes of human blood cells. J. Cell. Biol. 20: 37– 55. German, J., Lejeune, J., Macintyre, M. N. and Degrouchy, J. 1964. Chromosomal autoradiography in the Cri du Chat syndrome. Cytogenetics 3: 347– 352. Miller, O. J., Mukherjee, B. B., Breg, W. R. and Gamble, A. van N. 1963. Non-random distribution of chromosomes in metaphase figures from cultured huma leucocytes. I. The peripheral location of the Y chromosome. Cytogenetics 2: 1– 14. Mittwoch, U. and Delhanty, J. D. A. 1961. Nuclear sex in triploid XXY human cells. Lancet ii: 552. Moorhead, P. S. and Defendi, V. 1963. Asynchrony of DNA synthesis in chromosomes of human diploid cells. J. Cell. Biol. 16: 202– 209. Saksela, E. and Moorhead, P. S. 1962. Enhancement of secondary constrictions and the heterochromatic X in human cells. Cytogenetics 1: 225– 244. Schmid, W. 1963. DNA replication patterns of human chromosomes. Cytogenetics 2: 175– 193. Yunis, J. J., Hook, E. B. and Mayer, M. 1964. Deoxyribonucleic-acid replication pattern of trisomy D1 Lancet ii: 935– 936. Citing Literature Volume55, Issue1August 1966Pages 55-67 ReferencesRelatedInformation" @default.
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• W1994579911 title "CHROMOSOME DNA SYNTHESIS IN THE CELLS OF A HUMAN TRIPLOID/DIPLOID MOSAIC" @default.
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