Author:
Clayton P. T.,Kalter D. Chester,Atherton D. J.,Besley G. T. N.,Broadhead D. M.
Reference5 articles.
1. Besley, G. T. N. and Broadhead, D. M. Dihdroxyacetone phosphate acyl transferase deficiency in peroxisomal disorders. J. Inher. Metab. Dis. 10 Suppl. 2 (1987) 236–238
2. Clayton, P. T., Lake, B. D., Hall, N. A., Shortland, D. B., Carruthers, R. A. and Lawson, A. M. Plasma bile acids in patients with peroxisomal dysfunction syndromes; analysis by capillary gas chromatography–mass spectrometry. Eur. J. Pediatr. 146 (1987) 166–173
3. Happle, R. Cataracts as a marker of genetic heterogeneity in chondrodysplasia punctata. Clin. Genet. 19 (1981) 64–66
4. Holmes, R. D., Wilson, G. N. and Hajra, A. K. Peroxisomal enzyme deficiency in the Conradi-Hünermann form of chondrodysplasia punctata. (Letter) N. Engl. J. Med. 316 (1987) 1608
5. Schutgens, R. B. H., Heymans, H. S. A., Wanders, R. J. A., Van der Bosch, H. and Tager, J. M. Peroxisomal disorders: a newly recognised group of genetic diseases. Eur. J. Pediatr. 144 (1986) 430–440
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