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16. Genetic defects in human purine and pyrimidine metabolism. Boss GR; Seegmiller JE Annu Rev Genet; 1982; 16():297-328. PubMed ID: 6297375 [No Abstract] [Full Text] [Related]
17. Orotic aciduria, homocystinuria, formiminoglutamic aciduria and megaloblastosis associated with the formiminotransferase/cyclodeaminase deficiency. Shin YS; Reiter S; Zelger O; Brünstler I; von Rücker A Adv Exp Med Biol; 1986; 195 Pt A():71-6. PubMed ID: 3728187 [No Abstract] [Full Text] [Related]
19. Neonatal diagnosis of orotic aciduria: an experience with one family. McClard RW; Black MJ; Jones ME; Young SR; Berkowitz GP J Pediatr; 1983 Jan; 102(1):85-8. PubMed ID: 6848734 [No Abstract] [Full Text] [Related]
20. Hereditary orotic aciduria: a defect of pyrimidine metabolism with cellular immunodeficiency. Girot R; Durandy A; Perignon JL; Griscelli C Birth Defects Orig Artic Ser; 1983; 19(3):313-6. PubMed ID: 6606448 [No Abstract] [Full Text] [Related] [Next] [New Search]