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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

✍ Scribed by 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


Publisher
Springer
Year
1986
Tongue
English
Weight
254 KB
Volume
9
Category
Article
ISSN
0141-8955

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