METHOD AND COMPOSITIONS FOR THE IN VITRO DIAGNOSIS OF ILLNESSES DUE TO LYSOZOMIAL DEFICIENCIES OR CHROMOSOMAL ABERRATIONS, PARTICULARLY MUSCULAR DISTROPHY OR CYSTIC FIBROSIS

Process for in-vitro diagnosis of the potentiality or of the existence of cystic fibrosis, of muscular dystrophy or of a chromosome anomaly. It consists in placing a culture of cells originating from the individual or embryo being studied in contact with a cocktail comprising especially heparin, a h...

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