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Results: 1-3 |
Results: 3
Identification of a novel mutation in patients with medium-chain Acyl-CoA dehydrogenase deficiency
Authors: Yang, BZ Ding, JH Zhou, CC Dimachkie, MM Sweetman, L Dasouki, MJ Wilkinson, J Roe, CR
Citation: Bz. Yang et al., Identification of a novel mutation in patients with medium-chain Acyl-CoA dehydrogenase deficiency, MOL GEN MET, 69(3), 2000, pp. 259-262
Multiple inositol polyphosphate phosphatase: Evolution as a distinct groupwithin the histidine phosphatase family and chromosomal localization of the human and mouse genes to chromosomes 10q23 and 19
Authors: Chi, HB Tiller, GE Dasouki, MJ Romano, PR Wang, J O'Keefe, RJ Puzas, JE Rosier, RN Reynolds, PR
Citation: Hb. Chi et al., Multiple inositol polyphosphate phosphatase: Evolution as a distinct groupwithin the histidine phosphatase family and chromosomal localization of the human and mouse genes to chromosomes 10q23 and 19, GENOMICS, 56(3), 1999, pp. 324-336
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia
Authors: Ibdah, JA Dasouki, MJ Strauss, AW
Citation: Ja. Ibdah et al., Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia, J INH MET D, 22(7), 1999, pp. 811-814
Risultati: 1-3 |