Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
The Journal of Rheumatology|July 24, 1998
Bayesian calculation of methotrexate clearance after low dose intramuscular administration in patients with rheumatoid arthritisS Monjanel-Mouterde, P Lafforgue, A Blanc, et al.
Molecular Biology Reports|June 11, 1999
Are there multiple proteolytic pathways contributing to c-Fos, c-Jun and p53 protein degradation in vivo?C Salvat, C Aquaviva, I Jariel-Encontre, et al.
Human Mutation|August 29, 2001
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategyT Bienvenu, I Souville, K Poirier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]F Feillet, H Ogier, D Cheillan, et al.
Human Molecular Genetics|April 20, 2001
MECP2 is highly mutated in X-linked mental retardationP Couvert, T Bienvenu, C Aquaviva, et al.
Pageof 1