Medical genetics—genes and GPS for the 1990s
- 1 January 1993
- journal article
- review article
- Published by Wiley in Journal of Chemical Technology & Biotechnology
- Vol. 56 (2) , 123-134
- https://doi.org/10.1002/jctb.280560202
Abstract
DNA manipulation techniques have allowed the isolation and identification of many genes which cause disease in man. The same techniques are now being automated, and are on the threshold of application to more common and more complex genetic predispositions to diseases such as diabetes and schizophrenia. This article outlines the technology behind this development, and discusses some of the social, legal and ethical difficulties that widespread screening for genetic traits will raise. It is argued that these issues must be considered now, so that considered social responses to this technology are in place in the five years it is likely to take to develop. The techniques of DNA manipulation that have led to recombinant proteins and biopharmaceuticals have also led to an unprecedented increase in understanding of human genetics, and a corresponding increase in the practical side of human genetics—medical genetic diagnosis. As a result, medical genetics is moving from a speciality of statisticians and cytologists into the mainstream of medicine, and will soon be the concern of every hospital, and probably of every GP. This offers huge benefits to patients, but also threatens misunderstanding and even the potential of abuse if this sophisticated understanding of our fundamental natures is used without precision.Keywords
This publication has 63 references indexed in Scilit:
- Pharmacogenetics and ecogenetics in 1991Pharmacogenetics, 1991
- Breaking the fragile XNature, 1991
- Vision Assisted Robotics and Tape Technology in the Life-Science Laboratory: Applications to Genome AnalysisNature Biotechnology, 1990
- Complementary endeavoursNature, 1990
- Dominant susceptibility genesNature, 1990
- Psychological costs of screening.BMJ, 1989
- How informed is patients' consent to release of medical information to insurance companies?BMJ, 1989
- Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acidThe Journal of Pediatrics, 1988
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987
- New HLA DNA polymorphisms associated with autoimmune diseasesNature, 1986