Abstract
Virologists, pathologists, oncologists, immunologists and biochemists all use molecular genetic techniques as one of their investigative tools. Here, however, I shall restrict myself to molecular genetic investigations performed in a clinical genetics setting, but including tests for any clinical genetic purpose and not just antenatal diagnosis. These services are at present applicable only to diseases with a simple mendelian mode of inheritance.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
McKusick VA. Mendelian inheritance in man, 9th edn. Baltimore: Johns Hopkins, 1990.
Harris R, Elles R, Craufurd et al. Molecular genetics in the National Health Service in Britain. J Med Genet 1989; 26:219–25.
Rona RJ, Swan AV, Beech R et al. Demand for DNA probe testing in three genetic centres in Britain (August 1986 to July 1987). J Med Genet 1989; 26:226–36.
Landegren U, Kaiser R, Caskey CT, Hood L. DNA diagnostics — molecular techniques and automation. Science 1988; 242:229–37.
Cooper DN, Schmidtke J. Diagnosis of genetic disease using recombinant DNA, 2nd edn. Hum Genet 1989; 83:307–34.
Brock DJH. A consortium approach to molecular genetic services. J Med Genet 1990; 27:8–13.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1991 Springer-Verlag London Limited
About this chapter
Cite this chapter
Read, A.P. (1991). National Coordination of Molecular Genetic Services. In: Drife, J.O., Donnai, D. (eds) Antenatal Diagnosis of Fetal Abnormalities. Springer, London. https://doi.org/10.1007/978-1-4471-1854-1_24
Download citation
DOI: https://doi.org/10.1007/978-1-4471-1854-1_24
Publisher Name: Springer, London
Print ISBN: 978-1-4471-1856-5
Online ISBN: 978-1-4471-1854-1
eBook Packages: Springer Book Archive