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Results: 1-3 |
Results: 3

Authors: Chakrapani, A Olpin, S Cleary, M Walter, JH Wraith, JE Besley, GTN
Citation: A. Chakrapani et al., Trifunctional protein deficiency: Three families with significant maternalhepatic dysfunction in pregnancy not associated with E474Q mutation, J INH MET D, 23(8), 2000, pp. 826-834

Authors: Andresen, BS Olpin, S Kvittingen, EA Augoustides-Savvopoulou, P Lindhout, D Halley, DJJ Vianey-Saban, C Wanders, RJA IJlst, L Schroeder, LD Bolund, L Gregersen, N
Citation: Bs. Andresen et al., DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency, J INH MET D, 22(3), 1999, pp. 281-285

Authors: Andresen, BS Olpin, S Poorthuis, BJHM Scholte, HR Vianey-Saban, C Wanders, R Ijlst, L Morris, A Pourfarzam, M Bartlett, K Baumgartner, ER deKlerk, JBC Schroeder, LD Corydon, TJ Lund, H Winter, V Bross, P Bolund, L Gregersen, N
Citation: Bs. Andresen et al., Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency, AM J HU GEN, 64(2), 1999, pp. 479-494
Risultati: 1-3 |