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National Coordination of Molecular Genetic Services

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Book cover Antenatal Diagnosis of Fetal Abnormalities
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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.

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References

  1. McKusick VA. Mendelian inheritance in man, 9th edn. Baltimore: Johns Hopkins, 1990.

    Google Scholar 

  2. Harris R, Elles R, Craufurd et al. Molecular genetics in the National Health Service in Britain. J Med Genet 1989; 26:219–25.

    Article  PubMed  CAS  Google Scholar 

  3. 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.

    Article  PubMed  CAS  Google Scholar 

  4. Landegren U, Kaiser R, Caskey CT, Hood L. DNA diagnostics — molecular techniques and automation. Science 1988; 242:229–37.

    Article  PubMed  CAS  Google Scholar 

  5. Cooper DN, Schmidtke J. Diagnosis of genetic disease using recombinant DNA, 2nd edn. Hum Genet 1989; 83:307–34.

    Google Scholar 

  6. Brock DJH. A consortium approach to molecular genetic services. J Med Genet 1990; 27:8–13.

    Article  PubMed  CAS  Google Scholar 

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© 1991 Springer-Verlag London Limited

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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

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  • 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

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