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Results:
1-7
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Results: 7
Authors:
Erlandson, A
Hallberg, B
Hagberg, B
Wahlstrom, J
Martinsson, T
Citation: A. Erlandson et al., MECP2 mutation screening in Swedish classical Rett syndrome females, EUR CHILD A, 10(2), 2001, pp. 117-121
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:
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:
Matthijs, G
Schollen, E
Bjursell, C
Erlandson, A
Freeze, H
Imtiaz, F
Kjaergaard, S
Martinsson, T
Schwartz, M
Seta, N
Vuillaumier-Barrot, S
Westphal, V
Winchester, B
Citation: G. Matthijs et al., Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia), HUM MUTAT, 16(5), 2000, pp. 386-394
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:
Boone, T
Hansen, S
Erlandson, A
Citation: T. Boone et al., Cardiovascular responses to laughter: A pilot project, AP NURS RES, 13(4), 2000, pp. 204-208
Authors:
Erlandson, A
Alger, T
Horvath, J
Jancaitis, K
Lawson, J
Manes, K
Marshall, C
Moor, E
Payne, S
Pedrotti, L
Rodriguez, S
Rotter, M
Sutton, S
Zapata, L
Seznec, S
Beullier, J
Carbourdin, O
Grebot, E
Guenet, J
Guenet, M
LeTouze, G
Maille, X
Citation: A. Erlandson et al., Flashlamp-pumped Nd : glass amplifiers for the National Ignition Facility, FUSION TECH, 34(3), 1998, pp. 1105-1112
Risultati:
1-7
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