1. American Academy of Pediatrics, Committee on Genetics, Newborn screening fact sheets.Pediatrics 83 (1989) 449–464
2. Burlina, A. B., Sherwood, W. G., Marchiro, M. V. and Dalla Bernardina, B. Neonatal screening for biotinidase deficiency in north eastern Italy.Eur. J. Pediatr. 147 (1988) 317–318
3. Burri, B. J., Sweetmann, L. and Nyhan, W. L. Mutant holocarboxylase synthetase. Evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.J. Clin. Invest. 64 (1981) 1695–1702
4. Dunkel, G., Scriver, C. R., Clow, C. L., Melancon, S., Lemieux, B., Greiner, A. and Laberge, C. Prospective ascertainment of complete and partial serum biotinidase deficiency in the newborn.J. Inher. Metab. Dis. 12 (1989) 131–138
5. Havass, Z. Newborn screening programme for inborn errors of metabolism in East-Hungary. (Abstract).Clin. Genet. 28 (1985) 435