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• W2159138011 abstract "Journal of Intellectual Disability ResearchVolume 3, Issue 2 p. 78-87 AN UNUSUAL SEX CHROMATIN PATTERN IN THREE MENTALLY DEFICIENT SUBJECTS M. L. BARR, M. L. BARR Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this authorEVELYN L. SHAVER, EVELYN L. SHAVER Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this authorD. H. CARR, D. H. CARR Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this authorE. R. PLUNKETT, E. R. PLUNKETT Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this author M. L. BARR, M. L. BARR Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this authorEVELYN L. SHAVER, EVELYN L. SHAVER Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this authorD. H. CARR, D. H. CARR Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this authorE. R. PLUNKETT, E. R. PLUNKETT Departments of Microscopic Anatomy and Medical Research, University of Western Ontario, London, CanadaSearch for more papers by this author First published: December 1959 https://doi.org/10.1111/j.1365-2788.1959.tb00921.xCitations: 5AboutPDF ToolsRequest permissionExport 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 REFERENCES Bassermann, F. J. (1957). Zahl und Grösse der geschlechtsspezifischen Chromatin-differenziering in polyptoiden und endomitotisch verdoppelten Kernen von Flimmer-zellen des menschlichen Bronchialepithels. Arztl. Wschr, 12, 307. Beatty, R. A. (1957). Parthenogenesis and Polyploidy in Mammalian Development. Cambridge : University Press. Davidson, W. M. and Smith, D. R. (1954). A morphological sex difference in the poly-morphonuclear neutrophil leucocytes. Brit. med. J., 2, 6. Davidson, W. M, and Smith, D. R. (1958). The neutrophil sex nodules in Klinefelter's syndrome. P. 93 in Symposium on Nuclear Sex. London : William Heinemann-Medical Books Ltd. Ferguson-Smith, M. A. (1958). Chromatin-positive Klinefelter's syndrome (primary microrchidism) in in a mental deficiency hospital. Lancet, 1, 928. Ferguson-Smith, M. A. (1959), The prepubertal testicular lesion in chromatin-positive Klinefelter's syndrome (primary micro-orchidism) as seen in mentally handicapped children. Lancet. 1, 219. Ford, C. E., Jones, K. W., Miller, O. J., Mittwoch, U., Penrose, L. S., Ridler, M. and Shapiro. A.(1959 a). The chromosomes in a patient showing both mongolism and the Klinefelter syndrome. Lancet, 1, 709. Ford, C. E., Jones, K. W., Polani, P. E., DE Almeida, J. C. and Briggs. J. H. (1959 b). A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome). Lancet, 1, 711. Ford, C. E., Polani, P. E., Briggs, J. H. and Bishop, P. M. F. (1959 c). A presumptive human XXY/XX mosaic. Nature, Lond., 183, 1030. Jacobs, P. A., Baikie, A. G., Court Brown, W. M. and Strong, J. A. (1959). The somatic chromosomes in mongolism. Lancet, 1, 710. Jacobs, P. A. and Strong, J. A. (1959). A case of human intersexuality having a possible XXY sex-determining mechanism. Nature, Lond., 183, 302. Klinefelter, H. F., JR. (1958). Klinefelter's syndrome. P. 80 in Hermaphroditism, Genital Anomalies and Related Endocrine Disorders, by H. W. Jones, and W. W. Scott. Baltimore : The Williams and Wilkins Company. Klinger, H. P. (1958). The fine structure of the sex chromatin body. Exp. Cell Res, 14, 207. Klinger, H. P. and Sghwarzacher, H. G. (1958). Sex chromatin in polyploid nuclei of human amnion epithelium. Nature, Lond, 181, 1150. Kosenow, W. (1957). Abweichende Ergebnisse bei der Geschlechtsbestimmung an Leukozyten- und Mundepithel-Kernen. Klin. Wschr., 35, 75. Kosenow, W.(1958) Nutzen und Problematik der chromosomalen Geschlechtsdiagnose mit dem Leukozyten- und Mundepitheltest. Dtsch. med. Wichr., 83, 971. Lejeune, J., Gauthier, M. and Turpin, R. (1959). Les chromosomes humains en culture de tissus. C. R. Acad. Sci., Paris, 248, 602. Moore, K. L.(1959 a). Personal communication. Moore, K. L. (1959 h). Sex reversal in newborn babies. Lancet, 1, 217. Moore, K. L. and Barr, M. L. (1954). Nuclear morphology, according to sex, in human tissues. Act anat., 21, 197. Moore, K. L. and Barr, M. L. (1957). The sex chromatin in human malignant tissues. Brit. J. Cancer, 11, 384. Pasqualini, R. G., Vidal, G. and Bur, G. E. (1957). Psychopathology of Klinefelter's syndrome. Review of thirty-one cases. Lancet, 2, 164. Prader, A., Schneider, J., Frances, J. M. and Zublin, W. (1958 a). Frequency of the true (chromatin-positive) Klinefelter's syndrome. Lancet, 1, 968. Prader. A., Schneider, J., Zublin, W., Frances, J. M. and Ruedi, K. (1958 b). The frequency of the true, chromatin-positive Klinefelter-.syndrome and its relation to mental deficiency. Schweiz. med. Wschr., 88, 917. Reitalu, J.(1957) Observations on the so-called sex chromatin in man. Acta genet, med. gemellol., Roma, 6, 393. Serr, D. M., Ferguson-Smith, M. A., Lennox, B. and Paul, J. (1958). Representation of the X chromosome in intermitotic nuclei in man. Nature, Lond., 182, 124. Citing Literature Volume3, Issue2December 1959Pages 78-87 ReferencesRelatedInformation" @default.
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