1. Barr DGD, Kirk JM, Al Howasi M, Wanders RJA, Schutgens RBH (1993) Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency. Arch Dis Child 68:415–417
2. Batshaw ML, Thomas GH, Brusilow SW (1980) New approaches to the diagnosis and treatment of inborn errors of urea synthesis. Pediatrics 68:290–297
3. Beckman DR, Hoganson G, Berlow S, Gilbert EF (1987) Pathological findings in 5,10-methylenetetrahydrofolate reductase deficiency. Birth Defects 23:47–64
4. Berger R, Smit GPA, Schierbeek H, Bijsterveld K, le Coultre R (1985) Mevalonic aciduria: an inborn error of cholesterol biosynthesis? Clin Chim Acta 152 219–222
5. Brown GK (1994) Metabolic disorders of embryogenesis. J Inherit Metab Dis 17: 448–458