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Monosomies

  1. Jean-Pierre Fryns,
  2. Tshilobo Prosper Lukusa

Published Online: 27 JAN 2006

DOI: 10.1038/npg.els.0005545

eLS

eLS

How to Cite

Fryns, J.-P. and Lukusa, T. P. 2006. Monosomies. eLS. .

Author Information

  1. Centre for Human Genetics, Leuven, Belgium

Publication History

  1. Published Online: 27 JAN 2006

References

  1. References
  2. Further Reading
  3. Web Links
  • Angell RR (1997) First-meiotic-division nondisjunction in human oocytes. American Journal of Human Genetics 61: 2332.
  • Clement-Jones M, Schiller S, Rao E, et al. (2000) The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. Human Molecular Genetics 9: 695702.
  • Dailey T, Dale B, Cohen J and Munne S (1996) Association between nondisjunction and maternal age in meiosis-II human oöcytes. American Journal of Human Genetics 59: 176184.
  • Donnelly SL, Wolpert CM, Menold MM, et al. (2000) Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome. American Journal of Medical Genetics 96: 312316.
  • Guttenbach M, Koschorz B, Bernthaler U, Grimm T and Schmid M (1995) Sex chromosome loss and aging: in situ hybridization studies on human interphase nuclei. American Journal of Human Genetics 57: 11431150.
  • Hook EB (1983) Chromosome abnormalities and spontaneous fetal death following amniocentesis: further data and association with maternal age. American Journal of Human Genetics 35: 110116.
  • Powell CM (1999) Sex chromosomes and sex chromosome abnormalities. In: Gersen SL and Keagle MB (eds.) The Principles of Clinical Cytogenetics, pp. 229258. Totowa, NJ: Humana Press.

Further Reading

  1. References
  2. Further Reading
  3. Web Links

Web Links

  1. References
  2. Further Reading
  3. Web Links