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