Artigo Revisado por pares

Familial chromosomal mosaicism, genetic aspects

1970; Wiley; Volume: 33; Issue: 4 Linguagem: Inglês

10.1111/j.1469-1809.1970.tb01660.x

ISSN

1469-1809

Autores

Lillian Y. F. Hsu, Kurt Hirschhorn, Arthur I. Goldstein, Marcello A. Barcinski,

Tópico(s)

Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Resumo

Annals of Human GeneticsVolume 33, Issue 4 p. 343-349 Familial chromosomal mosaicism, genetic aspects LILLIAN Y. F. HSU, LILLIAN Y. F. HSU Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New YorkSearch for more papers by this authorKURT HIRSCHHORN, KURT HIRSCHHORN Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New York *K.H. is a Career Scientist of Health Research Council of the City of New York (1–513).Search for more papers by this authorARTHUR GOLDSTEIN, ARTHUR GOLDSTEIN Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New YorkSearch for more papers by this authorMARCELLO A. BARCINSKI, MARCELLO A. BARCINSKI Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New YorkSearch for more papers by this author LILLIAN Y. F. HSU, LILLIAN Y. F. HSU Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New YorkSearch for more papers by this authorKURT HIRSCHHORN, KURT HIRSCHHORN Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New York *K.H. is a Career Scientist of Health Research Council of the City of New York (1–513).Search for more papers by this authorARTHUR GOLDSTEIN, ARTHUR GOLDSTEIN Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New YorkSearch for more papers by this authorMARCELLO A. BARCINSKI, MARCELLO A. BARCINSKI Department of Pediatrics, Division of Medical Genetics and Department of Obstetrics and Gynecology, Mount Sinai School of Medicine, New York, New YorkSearch for more papers by this author First published: May 1970 https://doi.org/10.1111/j.1469-1809.1970.tb01660.xCitations: 27 AboutPDF 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 Beadle, G. W. (1932) A gene for sticky chromosomes in Zea Mays. Z. ind. Abstam. Vererbungsl. 63, 195–217. Bergemann, E. (1961) Manifestation familiale du karyotype triplo-X communication preliminaire. J. Hum, Genet. 10, 370–71. Borges, W. H., Wald, N. & Hoffman, E. (1964) Inherited cytogenetio mosaicism in man (Abstract). J. Pediat. 65, 103. Chicago Conference, 1966. Standardization in Human Gytogenetica: Birth Defects Original Article Series, vol. II, no. 2, December. Federman, D. D. (1967) Abnormal Sexual Development. A Genetic and Endocrine Approach to Differential Diagnosis, pp. 67–88. Chapter VI. Disorder of gonadal development, gonadal dysgenesis, dysgenetic male, pseudo hermaphroditism, agonadism. Philadelphia , Pa. : W. B. Saunders Company. Ferguson-Smith, M. A. (1965) Karyotype-phenotype correlations in gonadal dysgenesis and their bearing on the pathogenesis of malformations. J. Med. Genet. 2, 142–55. Ferrier, P. E., Ferrier, S. A., Scharer, K. O., Genton, N., Hedinger, Chr. & Klein, D. 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Program of the 46th Meeting. The Endocrine Society, June 18–20, 1964, San Francisco, p. 40 (Abstract 35). Rosenkranz, W. (1965) Familial mosaicism attributable to a new gene. Lancet i, 963–64. Rowley, J., Muldal, S., Lindsten, J. & Gilbert, C. W. (1964) H8-Thymidine uptake by a ring X chromosome in a human female. Proc. Nat. Acad. Sci. U.S.A. 51, 779–86. Sarles, H. E., Rodin, A. E., Poduska, P. R., Smith, G. H., Fish, J. C. & Remmers, A. R., Jr. (1968) Hereditary nephritis, retinitis pigmentosa and chromosomal abnormalities. Am. J. Med. 45, 312–21. Schachenmann, G., Schmid, W., Fraccaro, M., Mannini, A., Tiepolo, L., Perona, G. P. & Sartori, E. (1965) Chromosomes in coloboma and anal atresia. Lancet ii, 290. Schoen, E. J. (1965) Diminished testicular function in male Turner's syndrome. J. Clin. Endocrinol. 25, 101–13. Starkman, M. N. & Jaffe, R. B. (1967) Chromosome aberrations in XO/XY mosaic individuals and their fathers. Am. J. Obstet. Gynec. 99, 1056–66. Tips, R. L., Smith, G. S., Meyer, D. L. & Perkins, A. L. (1964) Familial mosaicism of a chromosome 16 abnormality associated with multiple congenital anomalies. Texas Am. J. Ment. Defic. 69, 330–40. Tzoneva-Maneva, M. T., Bosajieva, E. & Petrov, B. (1966) Chromosomal abnormalities in idiopathic osteoarthropathy. Lancet i, 1000–2. Walker, F. A. & Ising, R. (1969) Mosaic Down's syndrome in a father and daughter. Lancet i, 374. Weiss, L. & Wolf, C. B. (1968) Familial C/G translocation causing mitotic nondisjunction. Am. J. Dis. Child. 116, 609–14. Zellweger, H. & Abbo, G. (1965) Familial mosaicism attributable to a new gene. Lancet i, 455–7. Citing Literature Volume33, Issue4May 1970Pages 343-349 ReferencesRelatedInformation

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