Genesis of the Philadelphia chromosome: possible points of breakage in chromosome.

Abstract

HereditasVolume 79, Issue 2 p. 301-303 Open Access Genesis of the Philadelphia chromosome: Possible points of breakage in chromosome No. 22 Dimitrinka Pravtcheva, Corresponding Author Dimitrinka Pravtcheva Laboratory of Genetics, Centre of Oncology, Sofia, Bulgaria and Institute of Genetics, University of Lund, SwedenCentre of Oncology Sofia - Darvenitza BulgariaSearch for more papers by this authorGeorge Manolov, George Manolov Laboratory of Genetics, Centre of Oncology, Sofia, Bulgaria and Institute of Genetics, University of Lund, SwedenSearch for more papers by this author Dimitrinka Pravtcheva, Corresponding Author Dimitrinka Pravtcheva Laboratory of Genetics, Centre of Oncology, Sofia, Bulgaria and Institute of Genetics, University of Lund, SwedenCentre of Oncology Sofia - Darvenitza BulgariaSearch for more papers by this authorGeorge Manolov, George Manolov Laboratory of Genetics, Centre of Oncology, Sofia, Bulgaria and Institute of Genetics, University of Lund, SwedenSearch for more papers by this author First published: April 1975 https://doi.org/10.1111/j.1601-5223.1975.tb01487.xCitations: 2AboutPDF 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 Share a linkShare onFacebookTwitterLinkedInRedditWechat Literature cited Caspersson, T., Gahrton, G., Lindsten, J. and Zech, L. 1970. Identification of the Philadelphia chromosome as number 22 by quinacrine mustard fluorescence. Exp. Cell Res. 63: 238– 244. Lejeune, J. 1973. Scientific impact of the study of fine structure of chromatids. Nobel Symp. 23: 16– 24. Levan, A., Fredga, K. and Sandberg, A. A. 1964. Nomenclature for centromeric position on chromosomes. Hereditas 52: 201– 220. O'Riordan, M. L., Robinson, J. A., Buckton, K. E. and Evans, H. J. 1971. Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and chronic myeloid leukemia (Ph1) by fluorescence. Nature 230: 167– 168. Paris Conference 1971. Standardization in human cytogenetics. Birth defects: Original Article Series VIII: 7, 1972. The National Foundation, New York. Rowley, J. D. 1973. A new consistent chromosomal abnormality in chronic myelogenous leukemia identified by quinacrine fluorescence and Giemsa staining. Nature 243: 290– 293. Wang, H. C. and Fedoroff, S. 1972. Banding in human chromosomes treated with trypsin. Nature New Biol. 235: 52– 54. Whang-Peng, J., Lee, A. C. and Knutsen, T. A. 1974. Genesis of the Ph1 chromosome. J. Nat. Cancer Inst. 52: 1035– 1036. Citing Literature Volume79, Issue2April 1975Pages 301-303 ReferencesRelatedInformation