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Journal of Molecular Biology|April 9, 2001
A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definitionL J Fang, M J Simard, D Vidaud, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1979
Dicarboxylic amino acid uptake in normal, Friedreich's ataxia, and dicarboxylic aminoaciduria fibroblastsS B Melancon, B Grenier, L Dallaire, et al.
American Journal of Human Genetics|May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial diseaseC R Scriver, B Mahon, H L Levy, et al.
The Journal of Pediatrics|June 4, 1999
Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening programL C Sniderman, M Lambert, R Giguère, et al.
Bone Marrow Transplantation|March 23, 2004
Rituximab-related late-onset neutropenia after autologous stem cell transplantation for aggressive non-Hodgkin's lymphomaB Lemieux, S Tartas, C Traulle, et al.
The Plant Journal : for Cell and Molecular Biology|November 1, 1991
Identification and map position of YAC clones comprising one-third of the Arabidopsis genomeI Hwang, T Kohchi, B M Hauge, et al.
Muscle & Nerve|May 1, 1992
Human myoblast transplantation: preliminary results of 4 casesJ Huard, J P Bouchard, R Roy, et al.
Journal of Medical Genetics|November 4, 2008
Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15F-G Debray, M Lambert, B Lemieux, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|May 1, 1987
Feasibility of chemical screening of urine for neuroblastoma case finding in infancy in QuebecC R Scriver, D Gregory, M Bernstein, et al.
Cancer|December 1, 1995
Screening for neuroblastoma in North America. Preliminary results of a pathology review from the Quebec ProjectL A Takeuchi, Y Hachitanda, W G Woods, et al.
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