Identification by fluorescence of the G chromosome lost in human meningomas.

Abstract

HereditasVolume 71, Issue 1 p. 163-168 Open Access Identification by fluorescence of the G chromosome lost in human meningomas Joachim Mark, Corresponding Author Joachim Mark Institute of Pathology, Department of Neurosurgery and Institute of Genetics, University of Lund, SwedenInstitute of Pathology University of Lund S-22185 Lund, SwedenSearch for more papers by this authorGöran Levan, Göran Levan Institute of Pathology, Department of Neurosurgery and Institute of Genetics, University of Lund, SwedenSearch for more papers by this authorFelix Mitelman, Felix Mitelman Institute of Pathology, Department of Neurosurgery and Institute of Genetics, University of Lund, SwedenSearch for more papers by this author Joachim Mark, Corresponding Author Joachim Mark Institute of Pathology, Department of Neurosurgery and Institute of Genetics, University of Lund, SwedenInstitute of Pathology University of Lund S-22185 Lund, SwedenSearch for more papers by this authorGöran Levan, Göran Levan Institute of Pathology, Department of Neurosurgery and Institute of Genetics, University of Lund, SwedenSearch for more papers by this authorFelix Mitelman, Felix Mitelman Institute of Pathology, Department of Neurosurgery and Institute of Genetics, University of Lund, SwedenSearch for more papers by this author First published: June 1972 https://doi.org/10.1111/j.1601-5223.1972.tb01017.xCitations: 30AboutPDF 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 Benedict, W. F., Porter, I. H., Brown, C. D. and Florentin, R. A. 1970. Cytogenetic diagnosis of malignancy in recurrent meningioma. Lancet ( 1): 971– 973. Caspersson, T., Lomakka, G. and Zech, L. 1971. The 24 fluorescence patterns of the human metaphase chromosomes — distinguishing characters and variability. Hereditas 67: 89– 102. Mark, J. 1969. Two benign intracranial human tumours with an abnormal chromosomal picture. Acta Neuropathol. 14: 174– 184. Mark, J. 1970. Chromosomal patterns in human meningomas. Europ. J. Cancer 6: 489– 498. Mark, J. 1971. Chromosomal aberrations and their relation to malignancy in meningomas: A meningoma with ring chromosomes. Acta Pathol. Microbiol. Scand. 79: 193– 200. 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 leukaemia (Ph1) by fluorescence. Nature 230: 167– 168. Singer, H. and Zang, K. D. 1970. Cytologische und cytogenetische Untersuchungen and Hirntumoren. Humangenetik 9: 172– 184. Zang, K. D. and Singer, H. 1967. Chromosomal constitution of meningiomas. Nature 216: 84– 85. Citing Literature Volume71, Issue1June 1972Pages 163-168 ReferencesRelatedInformation