Artigo Revisado por pares

A CASE OF LIVEBORN TRIPLOIDY (69, XXX)

1972; Wiley; Volume: 61; Issue: 2 Linguagem: Inglês

10.1111/j.1651-2227.1972.tb15925.x

ISSN

1651-2227

Autores

E. Niebuhr, S. SPARREVOHN, K. Henningsen, Margareta Mikkelsen,

Tópico(s)

Parvovirus B19 Infection Studies

Resumo

Acta PaediatricaVolume 61, Issue 2 p. 203-208 A CASE OF LIVEBORN TRIPLOIDY (69, XXX) E. NIEBUHR, Corresponding Author E. NIEBUHR John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkJohn F. Kennedy Institute, Glostrup, Copenhagen, DenmarkSearch for more papers by this authorS. SPARREVOHN, S. SPARREVOHN John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkSearch for more papers by this authorK. HENNINGSEN, K. HENNINGSEN John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkSearch for more papers by this authorMARGARETA MIKKELSEN, MARGARETA MIKKELSEN John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkSearch for more papers by this author E. NIEBUHR, Corresponding Author E. NIEBUHR John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkJohn F. Kennedy Institute, Glostrup, Copenhagen, DenmarkSearch for more papers by this authorS. SPARREVOHN, S. SPARREVOHN John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkSearch for more papers by this authorK. HENNINGSEN, K. HENNINGSEN John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkSearch for more papers by this authorMARGARETA MIKKELSEN, MARGARETA MIKKELSEN John F. Kennedy Institute, Glostrup, the Paediatric Department of the Copenhagen County Hospital at Glostrup, and the Blood Group Department, Institute of Forensic Medicine, University of Copenhagen, DenmarkSearch for more papers by this author First published: March 1972 https://doi.org/10.1111/j.1651-2227.1972.tb15925.xCitations: 21AboutPDF 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 Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Atkins, L., Böök, J. A. & Santesson, B.: Chromosome DNA synthesis in the cells of a human tripoloid/diploid mosaic. Hereditas, 5: 55, 1966. 2 Bernard, R., Stahl, A., Coignet, J., Giraud, F., Hartung, M., Brusquet, Y. & Passeron, P.: Triploidie chromosomique chez un nouveau-né polymalformé. Ann Genet, 10: 70, 1967. 3 Bomsel-Helmreich, O.: Heteroploidy and embryonic death, in G. E. W. Wolstenholmes, (ed.): Preimplantation stages of pregnancy. Ciba Foundation Symposium, Churchill , London 1965, p. 246. 4 Boué, J. G. & Boué, A.: Fréquence des aberrations chromosomiques dans les avortements spontanés humains. C R Acad Sci (Paris), 269: 283, 1969. 5 Butler, J. L., Chantler, C., France, N. E. & Keith, C. G.: A liveborn infant with complete triploidy (69, XXX). J Med Genet, 6: 413, 1969. 6 Böök, J. A. & Santesson, B.: Malformation syndrome in man associated with triploidy (69 chromosomes). Lancet, 1: 858, 1960. 7 Böök, J. A., Masterson, J. G. & Santesson, B.: Malformation syndrome associated with triploidy. Further chromosome studies of the patient and his family. Acta Genet (Basel), 12: 193, 1962. 8 Carr, D. H.: Chromosome studies in spontaneous abortions. Obstet Gynec, 26: 308, 1965. 9 Carr, D. H.: Chromosomal errors and development. Amer J Obstet Gynec, 104: 327, 1969. 10 Edwards, J. H., Yuncken, C., Rushton, D. I., Richards, S. & Mittwoch, U.: Three cases of triploidy in man. Cytogenetics, 6: 81, 1967. 11 Ellis, J. R., Marshall, R., Normand, I. C. S. & Penrose, L. S.: A girl with triploid cells. Nature, 198: 411, 1963. 12 Ferrier, P., Stalder, G., Bamatter, F., Ferrier, S., Bühler, E. & Klein, D.: Congenital asymmetry associated with diploid-triploid mosaicism and large satellites. Lancet, 1: 80, 1964. 13 Frøland, A.: Photographic recording and dye staining of chromosomes for autoradiography and morphology. Stain Technol, 40: 42, 1965. 14 Keutel, J., Dollmann, A. & Münster, W.: Triploidie (69,XXY) bei einem lebend geborenen Kind. Z Kinderheilk, 109: 104, 1970. 15 Lejeune, J., Salmon, Ch., Berger, R., Réthoré, M. O., Rossier, A. & Job, J. C.: Chimére 46, XX/69, XXY. Ann Genet, 10: 188, 1967. 16 Mittwoch, U., Atkin, N. B. & Ellis, J. R.: Barr bodies in triploid cells. Cytogenetics, 2: 323, 1963. 17 Moorhead, P. S., Nowell, P. C., Mellman, W. J., Battips, D. M. & Hungerford, D. A.: Chromosome preparations of leucocytes cultured from human peripheral blood. Exp Cell Res, 20: 613, 1960. 18 Papiernik-Berkhauer, M. E.: Enfant triploïde a terme et thérapeutique hormonale. Bull Soc Nat Gynéc Obstét, 20: 248, 1968. 19 Rumpler, Y., Ruch, J. V. & Gerlinger, P.: Etude chromosomique de sujets porteurs de malformations ou présentant de syndromes cliniques congénitaux. Strasbourg Med, 4: 340, 1966. 20 Sacrez, R., Clavert, J., Willard, D., Rumpler, Y., M'Bede, J., Meyer, R. & Korn, R.: La Triploïdie chez l'enfant. Pediatrie, 22: 267, 1967. 21 Schindler, A. & Mikamo, K.: Triploidy in man. Cytogenetics, 9: 116, 1970. 22 Schmid, W. & Vischer, D.: A malformed boy with double aneuploidy and diploid-triploid mosaicism 48, XXYY/71, XXXYY. Cytogenetics, 6: 145, 1967. Citing Literature Volume61, Issue2March 1972Pages 203-208 ReferencesRelatedInformation

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