DOI: 10.1007/bf00273323. 45,X/46,XYq dic-Geschlechtschromosomenmosaik

45,X/46,XYq dic-Geschlechtschromosomenmosaik

10.1007/bf00273323

Crossref journal-article

Springer Science and Business Media LLC

Humangenetik (297)

Bibliography

Frey, R. O., BÃ¼hler, E. M., BÃ¼hler, U. K., & Stalder, G. R. (1975). 45,X/46,XYq dic-Geschlechtschromosomenmosaik. Humangenetik, 27(2), 81â90.

Authors 4

R. O. Frey (first)
E. M. Bühler (additional)
U. K. Bühler (additional)
G. R. Stalder (additional)

References 25 Referenced 54

Angell, R., Giannelli, F., Polani, P. E.: Three dicentric Y-chromosomes. Ann. hum. Genet. 34, 39–50 (1970) (10.1111/j.1469-1809.1970.tb00218.x) / Ann. hum. Genet. by R. Angell (1970)
Armendares, S., Buentello, L., Salamanca, F., Cantu-Garza, J. M.: A dicentric Y-chromosome without evidence of sexchromosomal mosaicism, 46,XYq dic, in a patient with features of Turner's syndrom. J. med. Genet. 9, 96–131 (1972) (10.1136/jmg.9.1.96) / J. med. Genet. by S. Armendares (1972)
Böök, J. A., Eilon, B., Halbrecht, I., Komlos, L., Shabtay F.: Isochromosome Y 46,X,i(Yq) and female phenotype. Clin. Genet. 4, 411–414 (1973) / Clin. Genet. by J. A. Böök (1973)
Boschetti, R., Gilbertas, A., Noel, B., Quack, B.: Pseudohermaphrodisme masculin et mosaique 46,X/46,XYdic/46,XXq-. Ann. Génét. 11, 62–65 (1968) / Ann. Génét. by R. Boschetti (1968)
Bühler, E. M., Frey, R., Müller, H., Voegelin, M., Stalder, G. R.: Fluorescence pattern of a dicentric Y. Humangenetik 12, 170–172 (1971a) / Humangenetik by E. M. Bühler (1971)
Bühler, E. M., Müller, H., Stalder, G. R.: Heterochromatin, Fluoreszenz und Struktur-Anomalien des Y-Chromosoms. Arch. Genet. 45, 27–34 (1972) / Arch. Genet. by E. M. Bühler (1972)
Bühler, E. M., Müller, H., Stalder, G. R., Werder, E.: A strongly fluorescing abnormal chromosome in a malformed child. Humangenetik 12, 64–66 (1971b) / Humangenetik by E. M. Bühler (1971)
Caspersson, T., Farber, S., Foley, G. E., Kudynowski, J., Modest, E. J., Simonsson, E., Wagh, U., Zech, L.: Chemical differentiation along metaphase chromosomes. Exp. Cell Res. 49, 219–222 (1968) (10.1016/0014-4827(68)90538-7) / Exp. Cell Res. by T. Caspersson (1968)
Caspersson, T., Zech, L., Johansson, C.: Differential binding of alkylating fluorochromes in human chromosomes. Exp. Cell Res. 60, 315–319 (1970) (10.1016/0014-4827(70)90523-9) / Exp. Cell Res. by T. Caspersson (1970)
Conen, P. E., Bailey, J. D., Allemang, W. H., Thompson, D. W., Ezrin, C.: A probable partial deletion of the Y-chromosome in an intersex patient. Lancet 1961 II, 294–295 (10.1016/S0140-6736(61)90582-7)
De la Chapelle, A., Wennström, J., Hortling, H., Ockey, C. H.: Isochromosome-X in man, Part I. Hereditas (Lund) 54, 260–276 (1966) (10.1111/j.1601-5223.1966.tb02021.x) / Hereditas (Lund) by A. De la Chapelle (1966)
Ferguson-Smith, M. A.: Karyotype-phenotype correlations in gonadal dysgenesis and their bearings on the pathogenesis of malformations. J. med. Genet. 2, 142–155 (1965) (10.1136/jmg.2.2.142) / J. med. Genet. by M. A. Ferguson-Smith (1965)
Ferguson-Smith, M. A., Boyd, E., Ferguson-Smith, M. E., Pritchard, J. G., Yusuf, A. F. M., Gray, B.: Isochromosome for long arm of Y chromosome in patient with Turner's syndrom and sex chromosome mosaicism (45,X/46,XYqi). J. med. Genet. 6, 422–425 (1969) (10.1136/jmg.6.4.422) / J. med. Genet. by M. A. Ferguson-Smith (1969)
Ferrier, P. E., Ferrier, S. A., Bill, A. H.: A male pseudohermaphrodite with a dicentric Y-chromosome. Humangenetik 6, 131–141 (1968) / Humangenetik by P. E. Ferrier (1968)
Hirschhorn, K., Decker, W. H., Cooper, H. L.: Human intersex with chromosome mosaicism of type XY/X0. New Engl. J. Med. 263, 1044 (1960) (10.1056/NEJM196011242632102) / New Engl. J. Med. by K. Hirschhorn (1960)
Jacobs, P. A., Ross, A.: Structural abnormalities of the Y-chromosome in man. Nature (Lond.) 210, 352–354 (1966) (10.1038/210352a0) / Nature (Lond.) by P. A. Jacobs (1966)
Jalbert, P., Couvert, A., Mouriquand, C., Malka, J.: A propos d'une observation d'Y dicentrique chez un pseudohermaphrodite masculin avec mosaique gonosomale complexe. Ann. Génét. 12, 253–258 (1969) / Ann. Génét by P. Jalbert (1969)
Mc Jlree, M. E. Price, W. H., Court-Brown, W. M., Tulloch, W. S., Newsam, J. E., Maclean, N.: Chromosome studies on testioular cells from 50 subfertile men. Lancet 1966 II, 69–71 (10.1016/S0140-6736(66)91803-4)
Nars, P. W., Bühler E. M. Das XO/XY Geschlechtschromosomen-Mosaik. Humangenetik 7, 185–196 (1969) / Humangenetik by P. W. Nars (1969)
Pearson, P. L., Bobrow, M.: Definitive evidence for the short arm of the Y-chromosome associating with the X-chromosome during meiosis in the human male. Nature (Lond.) 226, 959–961 (1970) (10.1038/226959a0) / Nature (Lond.) by P. L. Pearson (1970)
Siebers, J. W., Vogel, W., Hepp, H., Dittrich, A., Bolze, H.: Structural aberrations of the Y-chromosome and the corresponding phenotype. Report of a case with karyotype 45,X/46,X,i(Yp). Humangenetik 19, 57–66 (1973) (10.1007/BF00295235) / Humangenetik by J. W. Siebers (1973)
Starkman, M. N., Jaffé, R. B.: Chromosome aberrations in XO/XY mosaic individuals and their fathers. Amer. J. Obstet. Gynec. 99, 1056–1066 (1967) (10.1016/0002-9378(67)90343-2) / Amer. J. Obstet. Gynec. by M. N. Starkman (1967)
Yosa, C. G.: Heterochromatin recognition with fluorochromes. Chromosoma (Berl.) 30, 366–372 (1970) (10.1007/BF00321068) / Chromosoma (Berl.) by C. G. Yosa (1970)
Ying, K. L., Ives, E. J.: Mitotic behaviour of a human dicentric Y-chromosome. Cytogenetics 10, 208–218 (1971) (10.1159/000130140) / Cytogenetics by K. L. Ying (1971)
Yunis, J. J.: Human chromosome methodology, p. 187. New York-London: Academic Press 1965 (10.1016/B978-1-4832-3194-5.50016-5) / Human chromosome methodology by J. J. Yunis (1965)

Dates

Type	When
Created	3 years, 3 months ago (May 9, 2022, 4:04 a.m.)
Deposited	3 years, 3 months ago (May 9, 2022, 4:04 a.m.)
Indexed	1 year, 5 months ago (March 27, 2024, 12:36 a.m.)
Issued	50 years, 3 months ago (June 1, 1975)
Published	50 years, 3 months ago (June 1, 1975)
Published Print	50 years, 3 months ago (June 1, 1975)

Funders 0

None

BibTeX

@article{Frey_1975, title={45,X/46,XYq dic-Geschlechtschromosomenmosaik}, volume={27}, ISSN={0018-7348}, url={http://dx.doi.org/10.1007/bf00273323}, DOI={10.1007/bf00273323}, number={2}, journal={Humangenetik}, publisher={Springer Science and Business Media LLC}, author={Frey, R. O. and Bühler, E. M. and Bühler, U. K. and Stalder, G. R.}, year={1975}, month=jun, pages={81–90} }

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    "date-parts": [
      [
        1975,
        6
      ]
    ]
  },
  "references-count": 25,
  "journal-issue": {
    "issue": "2",
    "published-print": {
      "date-parts": [
        [
          1975,
          6
        ]
      ]
    }
  },
  "alternative-id": [
    "BF00273323"
  ],
  "URL": "http://dx.doi.org/10.1007/BF00273323",
  "relation": {},
  "ISSN": [
    "0018-7348"
  ],
  "subject": [],
  "container-title-short": "Hum Genet",
  "published": {
    "date-parts": [
      [
        1975,
        6
      ]
    ]
  }
}