Author: "Dekker, C. A." / Journal: journal of inherited metabolic disease - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"Dekker, C. A."' showing total 5 results

Start Over Author "Dekker, C. A." Journal journal of inherited metabolic disease

5 results on '"Dekker, C. A."'

1. Disorders of peroxisome biogenesis: Complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)

Author: Wanders, R. J. A., primary, Mooijer, P. A. W., additional, Dekker, C., additional, Suzuki, Y., additional, and Shimozawa, N., additional
Published: 1999
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2. X‐linked adrenoleukodystrophy: Improved prenatal diagnosis using both biochemical and immunological methods

Author: Wanders, R. J. A., primary, Mooyer, P. W., additional, Dekker, C., additional, and Vreken, P., additional
Published: 1998
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3. Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cells

Author: Wanders, R. J. A., primary, Ofman, R., additional, Romeijn, G. J., additional, Schutgens, R. B. H., additional, Mooijer, P. A. W., additional, Dekker, C., additional, and van den Bosch, H., additional
Published: 1995
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4. Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients

Author: Wanders, R. J. A., primary, Dekker, C., additional, Ofman, R., additional, Schutgens, R. B. H., additional, and Mooijer, P., additional
Published: 1995
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5. Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder

Author: Wanders, R. J. A., primary, Dekker, C., additional, Hovarth, V. A. P., additional, Schutgens, R. B. H., additional, Tager, J. M., additional, van Laer, P., additional, and Lecoutere, D., additional
Published: 1994
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