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

Research output: Contribution to journalArticlepeer-review

Original languageEnglish (US)
Pages (from-to)317-320
Number of pages4
JournalJournal of Inherited Metabolic Disease
Volume9
Issue number2 Supplement
DOIs
StatePublished - Jun 1986

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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