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:
Prip-Buus, C
Thuillier, L
Abadi, N
Prasad, C
Dilling, L
Klasing, J
Demaugre, F
Greenberg, CR
Haworth, JC
Droin, V
Kadhom, N
Gobin, S
Kamoun, P
Girard, J
Bonnefont, JP
Citation: C. Prip-buus et al., Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite community, MOL GEN MET, 73(1), 2001, pp. 46-54
Authors:
Prasad, C
Johnson, JP
Bonnefont, JP
Dilling, LA
Innes, AM
Haworth, JC
Beischel, L
Thuillier, L
Prip-Buus, C
Singal, R
Thompson, JRG
Prasad, AN
Buist, N
Greenberg, CR
Citation: C. Prasad et al., Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): Evidence for a founder effect andresults of a pilot study on a DNA-based newborn screening program, MOL GEN MET, 73(1), 2001, pp. 55-63
Authors:
Moroz, SP
Hadorn, B
Rossi, TM
Haworth, JC
Citation: Sp. Moroz et al., Celiac disease in a patient with a congenital deficiency of intestinal enteropeptidase, AM J GASTRO, 96(7), 2001, pp. 2251-2254
Citation: Ae. Chudley et Jc. Haworth, Genetic landmarks through philately - porphyria and its effect on world history, CLIN GENET, 55(2), 1999, pp. 85-87