Prenatal and perinatal diagnosis of peroxisomal disorders
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF01799291
Reference82 articles.
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3. Barth, P. G., Schutgens, R. B. H., Bakkeren, J. A. J. M., Dingemans, K. P., Heymans, H. S. A., Douwes, A. C. and van der Kley-van Moorsel, J. J. A milder variant of Zellweger syndrome.Eur. J. Pediatr. 144 (1985) 338–342
4. Beard. M. E., Baker, R., Conomos, P., Pugatch, D. and Holzman, E. Oxidation of oxalate and polyamines by rat liver peroxisomes.J. Histochem. Cytochem. 33 (1985) 460–464
5. Björkhem, I., Blomstrand, S., Glaumann, H. and Strandvik, B. Unsuccessful attempts to induce peroxisomes in two cases of Zellweger disease by treatment with clofibrate.Pediatr. Res. 19 (1985) 590–593
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