Authors:
Lemieux, B
Boivin, M
Brossard, JH
Lepage, R
Picard, D
Rosseau, L
D'Amour, P
Citation: B. Lemieux et al., Normal parathyroid function with decreased bone mineral density in treatedceliac disease, CAN J GASTR, 15(5), 2001, pp. 302-307
Authors:
Brodeur, GM
Look, AT
Shimada, H
Hamilton, VM
Maris, JM
Hann, HW
Leclerc, JM
Bernstein, M
Brisson, LC
Brossard, J
Lemieux, B
Tuchman, M
Woods, WG
Citation: Gm. Brodeur et al., Biological aspects of neuroblastomas identified by mass screening in Quebec, MED PED ONC, 36(1), 2001, pp. 157-159
Authors:
Fang, LJ
Simard, MJ
Vidaud, D
Assouline, B
Lemieux, B
Vidaud, M
Chabot, B
Thirion, JP
Citation: Lj. Fang et al., A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definition, J MOL BIOL, 307(5), 2001, pp. 1261-1270
Citation: D. Cyr et al., Determination of urinary acylcarnitines: A complementary aid for the high-risk screening of several organic acidurias using a simple and reliable GC/MS-based method, CLIN BIOCH, 33(2), 2000, pp. 151-155
Authors:
Cho, RJ
Mindrinos, M
Richards, DR
Sapolsky, RJ
Anderson, M
Drenkard, E
Dewdney, L
Reuber, TL
Stammers, M
Federspiel, N
Theologis, A
Yang, WH
Hubbell, E
Au, M
Chung, EY
Lashkari, D
Lemieux, B
Dean, C
Lipshutz, RJ
Ausubel, FM
Davis, RW
Oefner, PJ
Citation: Rj. Cho et al., Genome-wide mapping with biallelic markers in Arabidopsis thaliana, NAT GENET, 23(2), 1999, pp. 203-207
Authors:
Dupre, N
Bouchard, JP
Cossette, L
Brunet, D
Vanasse, M
Lemieux, B
Mathon, G
Puymirat, J
Citation: N. Dupre et al., Clinical and electrophysiological study in French-Canadian population withCharcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication, CAN J NEUR, 26(3), 1999, pp. 196-200
Citation: Wg. Woods et al., Randomized controlled trials in population-based intervention studies are not always feasible, MED PED ONC, 33(4), 1999, pp. 360-361
Authors:
Sniderman, LC
Lambert, M
Giguere, R
Auray-Blais, C
Lemieux, B
Laframboise, R
Rosenblatt, DS
Treacy, EP
Citation: Lc. Sniderman et al., Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening program, J PEDIAT, 134(6), 1999, pp. 675-680
Authors:
Fang, LJ
Feingold, J
Lemieux, B
Thirion, JP
Citation: Lj. Fang et al., A novel and very peculiar HincII polymorphism in the 5 ' region of the human neurofibromatosis type 1 (NF1) gene, ANN GENET, 42(4), 1999, pp. 231-233