Project: Introduction and development of recombinant DNA-analysis in the study and diagnosis of human hereditary disorders.
- project duration
- 01-JAN-00 – 31-DEC-99
- Application of available recombinant DNA-technology in order to diagnose some of the more frequent monogenic disorders in human : use of relevant restriction fragment length polymorphism about the genes responsible for mucoviscidosis and for dystrophia musculorum progressiva and other hereditary disorders. Demonstration of submicroscopic deletions in the karyotype. Practical purposes : diagnosis and prenatal diagnosis.