Pre- and postnatal diagnosis of the cerebrohepato-renal (Zellweger) syndrome via a simple method directly demonstrating the presence of absence of peroxisomes in cultured skin fibroblasts, amniocytes or chorionic villi fibroblasts

R. J.A. Wanders, G. Schrakamp, H. van den Bosch, J. M. Tager, H. W. Moser, A. E. Moser, P. Aubourg, W. J. Kleijer, R. B.H. Schutgens

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