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<jats:p>The application of recombinant DNA technology to the study of human genetic disease promises to increase the scope for carrier detection and prenatal diagnosis. Here we summarize current experience with prenatal diagnosis of single-gene disorders by DNA analysis and highlight some of the technical and organizational problems that remain to be solved.</jats:p>

Original publication

DOI

10.1098/rstb.1988.0047

Type

Journal article

Journal

Philosophical Transactions of the Royal Society of London. B, Biological Sciences

Publisher

The Royal Society

Publication Date

15/06/1988

Volume

319

Pages

249 - 261