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Results:
1-22
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Results: 22
Authors:
Goudeau, B
Dagvadorj, A
Rodrigues-Lima, F
Nedellec, P
Casteras-Simon, M
Perret, E
Langlois, S
Goldfarb, L
Vicart, P
Citation: B. Goudeau et al., Structural and functional analysis of a new desmin variant causing desmin-related myopathy, HUM MUTAT, 18(5), 2001, pp. 388-396
Authors:
Hiller, HH
Langlois, S
Citation: Hh. Hiller et S. Langlois, The most important books/articles in Canadian sociology in the twentieth century: A report, CAN J SOC, 26(3), 2001, pp. 513-516
Authors:
Kuchinka, BD
Barrett, IJ
Moya, G
Sanchez, JM
Langlois, S
Yong, SL
Kalousek, DK
Robinson, WP
Citation: Bd. Kuchinka et al., Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy, PRENAT DIAG, 21(1), 2001, pp. 36-39
Authors:
Gingras, D
Bousquet-Gagnon, N
Langlois, S
Lachambre, MP
Annabi, B
Beliveau, R
Citation: D. Gingras et al., Activation of the extracellular signal-regulated protein kinase (ERK) cascade by membrane-type-1 matrix metalloproteinase (MT1-MMP), FEBS LETTER, 507(2), 2001, pp. 231-236
Authors:
Langlois, S
Citation: S. Langlois, A productive decade in the tradition of Canadian sociology, CAN J SOC, 25(3), 2000, pp. 391-397
Authors:
Langlois, S
Citation: S. Langlois, Paul Lazarsicia (1901-1976). Sociology from Vienna to New York, CAN J SOC, 25(1), 2000, pp. 118-120
Authors:
Lestou, VS
Desilets, V
Lomax, BL
Barrett, IJ
Wilson, RD
Langlois, S
Kalousek, DK
Citation: Vs. Lestou et al., Comparative genomic hybridization: A new approach to screening for intrauterine complete or mosaic aneuploidy, AM J MED G, 92(4), 2000, pp. 281-284
Authors:
Cogny-Van Weydevelt, F
Dandavino, R
Langlois, S
Boucher, A
Citation: F. Cogny-van Weydevelt et al., Cost analysis of kidney transplantation with cyclosporin A, TRANSPLAN P, 32(2), 2000, pp. 434-435
Authors:
Bendahhou, S
Cummins, TR
Hahn, AF
Langlois, S
Waxman, SG
Ptacek, LJ
Citation: S. Bendahhou et al., A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation, J CLIN INV, 106(3), 2000, pp. 431-438
Authors:
Penaherrera, MS
Barrett, IJ
Brown, CJ
Langlois, S
Yong, SL
Lewis, S
Bruyere, H
Howard-Peebles, PN
Kalousek, DK
Robinson, WP
Citation: Ms. Penaherrera et al., An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta, CLIN GENET, 58(6), 2000, pp. 436-446
Authors:
McFadden, DE
Langlois, S
Citation: De. Mcfadden et S. Langlois, Parental and meiotic origin of triploidy in the embryonic and fetal periods, CLIN GENET, 58(3), 2000, pp. 192-200
Authors:
Gardes, F
Gaubert, P
Langlois, S
Citation: F. Gardes et al., Poverty and convergence of convergence of consumers in Canada, CAN R SOC A, 37(1), 2000, pp. 1-27
Authors:
Langlois, S
Desvignes, M
Constans, JM
Revenu, M
Citation: S. Langlois et al., MRI geometric distortion: A simple approach to correcting the effects of non-linear gradient fields, J MAGN R I, 9(6), 1999, pp. 821-831
Authors:
Toffelmire, EB
Barrett, BJ
Fenton, SS
Ferguson, B
Halligan, P
Langlois, S
McCready, WG
Muirhead, N
Weir, RV
Citation: Eb. Toffelmire et al., Chapter 2: Clinical practice guidelines for the management of anemia coexistent with chronic renal failure, J AM S NEPH, 10, 1999, pp. S292-S296
Authors:
Fang, P
Lev-Lehman, E
Tsai, TF
Matsuura, T
Benton, CS
Sutcliffe, JS
Christian, SL
Kubota, T
Halley, DJ
Meijers-Heijboer, H
Langlois, S
Graham, JM
Beuten, J
Willems, PJ
Ledbetter, DH
Beaudet, AL
Citation: P. Fang et al., The spectrum of mutations in UBE3A causing Angelman syndrome, HUM MOL GEN, 8(1), 1999, pp. 129-135
Authors:
Dollfus, S
Brazo, P
Langlois, S
Gourevitch, R
Dassa, D
Besse, F
Van der Elst, A
Thibaut, F
Delamillieure, P
Chabot, B
Guelfi, JD
Petit, M
Citation: S. Dollfus et al., Month of birth in deficit and non-deficit schizophrenic patients, EUR PSYCHIA, 14(6), 1999, pp. 349-351
Authors:
Langlois, S
Lit, JWY
Citation: S. Langlois et Jwy. Lit, S-resonator with an end reflector, J LIGHTW T, 17(8), 1999, pp. 1487-1492
Authors:
Bernard, LE
Penaherrera, MS
Van Allen, MI
Wang, MS
Yong, SL
Gareis, F
Langlois, S
Robinson, WP
Citation: Le. Bernard et al., Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7: Comparison with non-UPD7 cases, AM J MED G, 87(3), 1999, pp. 230-236
Authors:
Bruyere, H
Lewis, MES
Wood, S
MacLeod, P
Langlois, S
Citation: H. Bruyere et al., Increasing evidence for a new X-linked mental retardation/epilepsy gene localized to Xp21.3-Xp22.1, AM J MED G, 86(4), 1999, pp. 401-401
Authors:
Bruyere, H
Lewis, S
Wood, S
MacLeod, PJ
Langlois, S
Citation: H. Bruyere et al., Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1, CLIN GENET, 55(3), 1999, pp. 173-181
Authors:
Yong, KN
Wadsworth, LD
Langlois, S
Yong, SL
Wilson, RD
Citation: Kn. Yong et al., Thalassemia carrier screening and prenatal diagnosis among the British Columbia (Canada) population of Chinese descent, CLIN GENET, 55(1), 1999, pp. 20-25
Authors:
Lavigne, C
Roblin, A
Outters, V
Langlois, S
Girasole, T
Roze, C
Citation: C. Lavigne et al., Comparison of iterative and Monte Carlo methods for calculation of the aureole about a point source in the Earth's atmosphere, APPL OPTICS, 38(30), 1999, pp. 6237-6246
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