Skip to main content

Prenatal Diagnosis

  • Chapter
Molecular Genetic Pathology

Abstract

Cytogenetic prenatal diagnosis involves examination of the fetal chromosome complement

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 149.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Suggested Reading

  • Cheung SW, Shaw CA, Yu W, et al. Development and validation of a CGH microarray for clinical cytogenetic diagnosis. Genet Med. 2005;7:422–432.

    Article  PubMed  Google Scholar 

  • Crolla JA. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature. Am J Med Genet. 1998;75(4):367–381.

    Article  CAS  PubMed  Google Scholar 

  • Evans MI, Wapner RJ. Invasive prenatal diagnostic procedures 2005. Semin Perinatol. 2005;29(4):215–218.

    Article  PubMed  Google Scholar 

  • Gardner RJM, Sutherland GR. Chromosome Abnormalities and Genetic Counseling. 3rd ed. New York, NY: Oxford University Press; 2004; p. 311–335, p. 392–432.

    Google Scholar 

  • Knight SJ, Lese CM, Precht KS, et al. An optimized set of human telomere clones for studying telomere integrity and architecture. Am J Hum Genet. 2000;67:320–332.

    Article  CAS  PubMed  Google Scholar 

  • Ledbetter DH, Engel E. Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. Hum Mol Genet. 1995;4:1757–1764.

    CAS  PubMed  Google Scholar 

  • Randolph LM. Prenatal Cytogenetics. In: Gersen SL, Keagle MB, eds. The Principles of Clinical Cytogenetics. Totowa: Humana Press; 2005;267–321.

    Google Scholar 

  • Shaffer LG. Risk estimates for uniparental disomy following prenatal detection of a nonhomologous Robertsonian translocation. Prenat Diagn. 2006;26:303–307.

    Article  PubMed  Google Scholar 

  • Tepperberg J, Pettenati MJ, Rao PN. Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH), 2-year multi-center retrospective study and review of the literature. Prenat Diagn. 2001;21:293–301.

    Article  CAS  PubMed  Google Scholar 

  • Warburton D. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. Am J Hum Genet. 1991;49(5):995–1013.

    CAS  PubMed  Google Scholar 

  • Wenstrom KD. Evaluation of Down syndrome screening strategies. Semin Perinatol. 2005;29(4):219–224.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2008 Humana Press, a part of Springer Science+Business Media, LLC

About this chapter

Cite this chapter

Kardon, N., Edelmann, L. (2008). Prenatal Diagnosis. In: Cheng, L., Zhang, D.Y. (eds) Molecular Genetic Pathology. Humana Press. https://doi.org/10.1007/978-1-59745-405-6_17

Download citation

  • DOI: https://doi.org/10.1007/978-1-59745-405-6_17

  • Publisher Name: Humana Press

  • Print ISBN: 978-1-58829-974-1

  • Online ISBN: 978-1-59745-405-6

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics