1. Antenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Issue 9 (September 1989) Authors: Strachan, T; Price, D A; Brook, C G D; Rumsby, G Journal: Archives of disease in childhood Issue: Volume 64:Issue 9(1989) Page Start: 1344 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia. Issue 3 (June 1986) Authors: Rumsby, G; Carroll, M C; Porter, R R; Grant, D B; Hjelm, M Journal: Journal of medical genetics Issue: Volume 23:Issue 3(1986) Page Start: 204 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency. Issue 9 (September 1988) Authors: Rumsby, G; Fielder, A H; Hague, W M; Honour, J W Journal: Journal of medical genetics Issue: Volume 25:Issue 9(1988) Page Start: 596 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. In vitro gene amplification for prenatal diagnosis of congenital adrenal hyperplasia. Issue 11 (November 1990) Authors: Rumsby, G; Honour, J W Journal: Journal of medical genetics Issue: Volume 27:Issue 11(1990) Page Start: 676 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing. Issue 9 (September 1996) Authors: Rumsby, G; Massoud, A F; Avey, C; Brook, C G Journal: Journal of medical genetics Issue: Volume 33:Issue 9(1996) Page Start: 798 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of the AGXT gene. Issue 6 (June 1997) Authors: von Schnakenburg, C; Rumsby, G Journal: Journal of medical genetics Issue: Volume 34:Issue 6(1997) Page Start: 489 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Primary hyperoxaluria type 3 in children with renal calculi. (4th April 2011) Authors: Williams, E; Bockenhauer, D; Smeulders, N; Barnacle, A; Choong, S; Rumsby, G; van't Hoff, W Journal: Archives of disease in childhood Issue: Volume 96(2011)Supplement 1 Page Start: A68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Rapid liquid chromatography tandem mass-spectrometry screening method for urinary metabolites of primary hyperoxaluria. (March 2019) Authors: Woodward, G; Pryke, R; Hoppe, B; Rumsby, G Journal: Annals of clinical biochemistry Issue: Volume 56:Number 2(2019:Mar.) Page Start: 232 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗