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Journal of Medical Genetics|June 1, 1986
Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasiaG Rumsby, M C Carroll, R R Porter, et al.Molecular Urology|January 13, 2001
Biochemical and genetic diagnosis of the primary hyperoxalurias: a reviewG RumsbyJournal of Nephrology|May 30, 1998
Experience in prenatal diagnosis of primary hyperoxaluria type 1G RumsbyAnnals of Clinical Biochemistry|February 17, 1998
Kinetic analysis and tissue distribution of human D-glycerate dehydrogenase/glyoxylate reductase and its relevance to the diagnosis of primary hyperoxaluria type 2C F Giafi, G RumsbyNeuroscience Letters|December 31, 1982
A syringe modification for the simple and rapid dissociation of post-natal rat cerebral tissue for preparing primary cultures of mixed glial cellsJ Chapman, M G RumsbyBiochimica Et Biophysica Acta|October 19, 1999
Identification and expression of a cDNA for human hydroxypyruvate/glyoxylate reductaseG Rumsby, D P CregeenJournal of the American Society of Nephrology : JASN|November 30, 1999
Recent developments in our understanding of primary hyperoxaluria type 2D P Cregeen, G RumsbyJournal of Neurochemistry|October 1, 1980
Accessibility of galactosyl ceramides to probe reagents in central nervous system myelinC Linington, M G RumsbyThe Journal of Steroid Biochemistry and Molecular Biology|April 1, 1993
Problems in diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyJ W Honour, G RumsbyScandinavian Journal of Haematology|August 1, 1980
Ageing of blood in hereditary spherocytosisC Little, M G RumsbyPageof 251