1. The Zellweger syndrome: book review and bibliography;Opitz, J.M.;Am J Med Genet; The cerebro-hepato-renal (Zellweger) syndrome and other peroxisomal disorders,1985
2. Complementation analysis of peroxisomal diseases by somatic cell fusion;Tager, J.M.; Westerveld, A.; Strijland, A.,1987
3. A milder variant of Zellweger syndrome;Barth, P.G.; Schutgens, R.B.H.; Bakkeren, J.A.J.M.;Eur J Pediatr,1985
4. Long-term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome;Bleeker-Wagemakers, E.M.; Oorthuys, J.W.E.; Wanders, R.J.A.; Schutgens, R.B.H.;Clin Genet,1986
5. Dysmorphic syndrome with phytanic oxidase deficiency, abnormal very long chain fatty acids, and pipecolicacidaemia: studies in four children;Budden, S.S.; Kennaway, N.G.; Buist, N.R.M.; Poulis, A.; Weleber, R.G.;J Pediatr,1986