1. Acute intermittent porphyria caused by defective splicing of porphobilinogen deaminase RNA: a synonymous codon mutation at -22 bp from the 5' splice site causes skipping of exon 3. Issue 5 (May 1996) Authors: Llewellyn, D H; Scobie, G A; Urquhart, A J; Whatley, S D; Roberts, A G; Harrison, P R; Elder, G H Journal: Journal of medical genetics Issue: Volume 33:Issue 5(1996) Page Start: 437 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Heterogeneity of familial porphyria cutanea tarda. Issue 10 (October 1988) Authors: Roberts, A G; Elder, G H; Newcombe, R G; Enriquez de Salamanca, R; Munoz, J J Journal: Journal of medical genetics Issue: Volume 25:Issue 10(1988) Page Start: 669 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Systemic lactose intolerance: a new perspective on an old problem. Issue 953 (4th March 2005) Authors: Matthews, S B; Waud, J P; Roberts, A G; Campbell, A K Journal: Postgraduate medical journal Issue: Volume 81:Issue 953(2005) Page Start: 167 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading. Issue 1 (16th January 2004) Authors: Livesey, K J; Wimhurst, V L C; Carter, K; Worwood, M; Cadet, E; Rochette, J; Roberts, A G; Pointon, J J; Merryweather-Clarke, A T; Bassett, M L; Jouanolle, A-M; Mosser, A; David, V; Poulton, J; Robson, K J H Journal: Journal of medical genetics Issue: Volume 41:Issue 1(2004) Page Start: 6 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗