1. Population screening for congenital hypothyroidism. Issue 6215 (8th March 1980) Authors: Hulse, J A; Grant, D B; Clayton, B E; Lilly, P; Jackson, D; Spracklan, A; Edwards, R W; Nurse, D Journal: BMJ Issue: Volume 280:Issue 6215(1980) Page Start: 675 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Hyperphenylalaninaemia of various types among three-quarters of a million neonates tested in a screening programme. Issue 10 (October 1981) Authors: Walker, V; Clayton, B E; Ersser, R S; Francis, D E; Lilly, P; Seakins, J W; Smith, I; Whiteman, P D Journal: Archives of disease in childhood Issue: Volume 56:Issue 10(1981) Page Start: 759 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Changing incidence of neonatal hypermethioninaemia: implications for the detection of homocystinuria. Issue 8 (August 1979) Authors: Whiteman, P D; Clayton, B E; Ersser, R S; Lilly, P; Seakins, J W Journal: Archives of disease in childhood Issue: Volume 54:Issue 8(1979) Page Start: 593 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗