Molecular studies of human genetic disease
- PMID: 1846832
- DOI: 10.1096/fasebj.5.1.1846832
Molecular studies of human genetic disease
Abstract
A wide variety of techniques are available for detecting disease-causing mutations within human genes; this report provides a brief review of such procedures. Good communication and exchange of materials between the clinical genetics field and the Human Genome Initiative will benefit both.
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