AAAAAA
Results:
1-7
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Results: 7
Authors:
Erlandson, A
Bjursell, C
Stibler, H
Kristiansson, B
Wahlstrom, J
Martinsson, T
Citation: A. Erlandson et al., Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations, HUM GENET, 108(5), 2001, pp. 359-367
Authors:
Helander, A
Eriksson, G
Stibler, H
Jeppsson, JO
Citation: A. Helander et al., Interference of transferrin isoform types with carbohydrate-deficient transferrin quantification in the identification of alcohol abuse, CLIN CHEM, 47(7), 2001, pp. 1225-1233
Authors:
Erlandson, A
Stibler, H
Kristiansson, B
Wahlstrom, J
Martinsson, T
Citation: A. Erlandson et al., Denaturing high-performance liquid chromatography is a suitable method forPMM2 mutation screening in carbohydrate-deficient glycoprotein syndrome type IA patients, GENET TEST, 4(3), 2000, pp. 293-297
Authors:
Bjursell, C
Erlandson, A
Nordling, M
Nilsson, S
Wahlstrom, J
Stibler, H
Kristiansson, B
Martinsson, T
Citation: C. Bjursell et al., PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families, HUM MUTAT, 16(5), 2000, pp. 395-400
Authors:
Van Setten, GB
Edstrom, L
Stibler, H
Rasmussen, S
Schultz, G
Citation: Gb. Van Setten et al., Levels of transforming growth factor alpha (TGF-alpha) in human cerebrospinal fluid, INT J DEV N, 17(2), 1999, pp. 131-134
Authors:
Stibler, H
Gylje, H
Uller, A
Citation: H. Stibler et al., A neurodystrophic syndrome resembling carbohydrate-deficient glycoprotein syndrome type III, NEUROPEDIAT, 30(2), 1999, pp. 90-92
Authors:
Bjursell, C
Wahlstrom, J
Berg, K
Stibler, H
Kristiansson, B
Matthijs, G
Martinsson, T
Citation: C. Bjursell et al., Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families, EUR J HUM G, 6(6), 1998, pp. 603-611
Risultati:
1-7
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