1. Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs. Issue 8 (August 1975) Authors: Pavone, L; Mollica, F; Levy, H L Journal: Archives of disease in childhood Issue: Volume 50:Issue 8(1975) Page Start: 637 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling. Issue 2 (February 1996) Authors: Guldberg, P; Levy, H L; Henriksen, K F; Guttler, F Journal: Journal of medical genetics Issue: Volume 33:Issue 2(1996) Page Start: 161 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗