Reassessing fecundity in women with classical congenital adrenal hyperplasia (CAH): normal pregnancy rate but reduced fertility rate von Casteràs, Anna, De Silva, Purnami, Rumsby, Gillian, Conway, Gerard S.

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Three Novel Deletions in the Alanine:Glyoxylate Aminotransferase Gene of Three Patients with Type 1 Hyperoxaluria von Coulter-Mackie, Marion B., Rumsby, Gillian, Applegarth, Derek A., Toone, Jennifer R.

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Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acne von Ostlere, Lucy S., Rumsby, Gillian, Holownia, Peter, Jacobs, Howard S., Rustin, Malcolm H. A., Honour, John W.

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STRATEGIES FOR THE PRENATAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1 von DANPURE, CHRISTOPHER J., RUMSBY, GILLIAN

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Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene von DANPURE, C. J, BIRDSEY, G. M, RUMSBY, G, LUMB, M. J, PURDUE, P. E, ALLSOP, J

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Primary hyperoxaluria type 1 caused by peroxisome-to-mitochondrion mistargeting of alanine : glyoxylate aminotransferase von LHOTTA, K, RUMSBY, G, VOGEL, W, PERNTHALER, H, FEICHTINGER, H, KÖNIG, P

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Effect of temperature and sample preparation on performance of ion-moderated partition chromatography of organic acids in biological fluids von Rumsby, Gillian, Belloque, Josefina, Ersser, Roger S., Seakins, James W.T.

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Expression of Genes on Human Chromosome 21a von DAVIDSON, JEFFREY N., RUMSBY, GILLIAN, NISWANDER, LEE A.

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Ornithine decarboxylase induction and the cytoskeleton in normal and transformed cells von Rumsby, Gillian, Puck, Theodore T.

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Expression of Genes on Human Chromosome 21 von DAVIDSON, JEFFREY N., RUMSBY, GILLIAN, NISWANDER, LEE A.

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Primary hyperoxaluria type 1 caused by peroxisome-to-mitochondrion mistargeting of alanine : glyoxylate aminotransferase von Lhotta, Karl, Rumsby, Gillian, Vogel, Wolfgang, Pernthaler, Heinz, Feichtinger, Hans, König, Paul

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