Skip to main content
PMC home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1974 Jan;26(1):83–92.

Apparently isodicentric but functionally monocentric X chromosome in man.

E Therman, G E Sarto, K Patau
PMCID: PMC1762552  PMID: 4130093

Full text

PDF
86

Images in this article

85Fig. 1
on p.85
87Fig. 2
on p.87
88Fig. 3
on p.88

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Cohen M. M., Lin C. C., Sybert V., Orecchio E. J. Two human X-autosome translocations identified by autoradiography and fluorescence. Am J Hum Genet. 1972 Sep;24(5):583–597. [PMC free article] [PubMed] [Google Scholar]
  2. Craig-Holmes A. P., Moore F. B., Shaw M. W. Polymorphism of human C-band heterochromatin. I. Frequency of variants. Am J Hum Genet. 1973 Mar;25(2):181–192. [PMC free article] [PubMed] [Google Scholar]
  3. DeMars R. The single-active-X: functional differentiation at the chromosome level. Natl Cancer Inst Monogr. 1967 Sep;26:327–351. [PubMed] [Google Scholar]
  4. Distèche C., Hagemeijer A., Frederic J., Progneaux D. An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry. Clin Genet. 1972;3(5):388–395. doi: 10.1111/j.1399-0004.1972.tb01472.x. [DOI] [PubMed] [Google Scholar]
  5. Emerit I., German J., Crippa L. P., Sureau C. Duplication d'un chromosome X dans un cas de syndrome de Turner (45,X-46XXp+) (45,X-46,XXp+) Ann Genet. 1970 Dec;13(4):245–248. [PubMed] [Google Scholar]
  6. Engel W., Vogel W., Reinwein H. Autoradiographische Untersuchungen an einer X-Autosomentranslokation beim Menschen: 45,X.15-,tan(15qXq+) Cytogenetics. 1971;10(2):87–98. [PubMed] [Google Scholar]
  7. Mukerjee D., Burdette W. J. Multiple congenital anomalies associated with a ring 3 chromosome and translocated 3/X chromosome. Nature. 1966 Oct 8;212(5058):153–155. doi: 10.1038/212153a0. [DOI] [PubMed] [Google Scholar]
  8. Neurath P. W., Lin P. S., Low D. A. Quantitative karyotyping: a model twin study. Cytogenetics. 1972;11(6):457–474. doi: 10.1159/000130213. [DOI] [PubMed] [Google Scholar]
  9. Niebuhr E. A 45,XX,5-,13-,dic+ karyotype in a case of cri-du-chat syndrome. Cytogenetics. 1972;11(3):165–177. doi: 10.1159/000130186. [DOI] [PubMed] [Google Scholar]
  10. Niebuhr E. Dicentric and monocentric Robertsonian translocations in man. Humangenetik. 1972;16(3):217–226. doi: 10.1007/BF00273467. [DOI] [PubMed] [Google Scholar]
  11. Sarto G. E., Therman E., Patau K. X inactivation in man: a woman with t(Xq--;12q+). Am J Hum Genet. 1973 May;25(3):262–270. [PMC free article] [PubMed] [Google Scholar]
  12. Thorburn M. J., Miller C. G., Dovey P. Anomalies of development in a girl with unusual sex chromosomal mosaicism. J Med Genet. 1967 Dec;4(4):283–287. doi: 10.1136/jmg.4.4.283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. WIELIE G., COENEGRACHT J. M., STALDER G. A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME. Cytogenetics. 1964;3:427–440. doi: 10.1159/000129831. [DOI] [PubMed] [Google Scholar]
  14. Warburton D., Henderson A. S., Shapiro L. R., Hsu L. Y. A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres. Am J Hum Genet. 1973 Jul;25(4):439–445. [PMC free article] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES