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Results: 3

Authors: Holzinger, A Maier, EM Buck, C Mayerhofer, PU Kappler, M Haworth, JC Moroz, SP Hadorn, HB Sadler, JE Roscher, AA
Citation: A. Holzinger et al., Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency, AM J HU GEN, 70(1), 2002, pp. 20-25

Authors: Randak, C Roschinger, W Rolinski, B Hadorn, HB Applegarth, DA Roscher, AA
Citation: C. Randak et al., Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria, J INH MET D, 23(5), 2000, pp. 520-522

Authors: Heinz-Erian, P Schmidt, H Le Merrer, M Phillips, AD Kiess, W Hadorn, HB
Citation: P. Heinz-erian et al., Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia, J PED GASTR, 28(2), 1999, pp. 203-205
Risultati: 1-3 |