1. Silver DN, Lewis RA, Nussbaum RL (1987) Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphisms. J Clin Invest 79:282–285
2. Wadelius C, Fagerholm P, Petterson U, et al. (1989) Lowe oculocerebrorenal syndrome. DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers as the correlation to lens examination in carrier diagnosis. Am J Hum Genet 44:241–247
3. Lowe CU, Terry M, MacLachlan EA (1952) Organic aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation: a clinical entity. Am J Dis Child 83:164–184
4. Glinsberg J, Bove KE, Fogelson MH (1981) Pathological features of the eye in the oculocerebrorenal (Lowe) syndrome. J Pediatr Ophthalmol Strabism 18:16–24
5. Charnas L, Bernar J, Pezeshkpour GH, et al. (1988) MRI findings and peripheral neurology in Lowe's syndrome. Neuro-pediatrics 19:7–9