Author:
Adolph K. J.,Fung E.,McLeod D. R.,Morgan K.,Snyder F. F.
Reference14 articles.
1. Lowry RB, Snyder FF, Wesenberg, RL, Machin GA, Applegarth DA, Morgan K, Carter RJ, Toone JR, Holmes TM and Dewar RD. Morquio Syndrome (MPS IVA) and hypophosphatasia in a Hutterite kindred. Am J Hum Genet 22: 463–475 (1985).
2. Fowlow SB, Holmes TM, Morgan K and Snyder FF. Screening for methylmalonic aciduria in Alberta: A voluntary program with particular significance for the Hutterite Brethren. Am J Med Genet 22: 513–519 (1985).
3. Bakkeren JAJM, De Abreu RA, Sengers RCA, Gabreels FJM, Maas JM, Reníer WO. Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiency. Clinica Chim Acta 140: 247–256 (1984).
4. Berger R, Stoker-de Vries SA, Wadman SK, Duran M, Beemer FA, de Bree PK, Weits-Binnerts JJ, Fenders TJ and van der Woude JK. Dihydropyrimidine dehydrogenase deficiency leading to thymineuraciluria. An inborn error of pyrimidine metabolism. Clinica Chim Acta 141: 227–234 (1984).
5. Suttle DP, Becroft DMO, Webster DR. Hereditary orotic aciduría and other disorders of pyrimidine metabolism. In “The Metabolic Basis of Inherited Disease”, Scriver CR et al. McGraw Hill 6th Edition, 11191121 (1989).
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