Showing results (11-20 of 31) with videos related to
Sort By:
Pageof 4
Nephrologie|January 1, 1994
[Molecular pathology of type 1 primary hyperoxaluria]P Cochat, M O Rolland, D Bozon, et al.FEBS Letters|July 31, 1989
Delta zero-thalassemia in cis of beta Knossos-globin gene. Normal structure transient expression of the delta-globin geneR Ouazana, D Bozon, F Baklouti, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|February 8, 2003
Mucopolysaccharidosis type II--genotype/phenotype aspectsR Froissart, I Moreira da Silva, N Guffon, et al.Molecular and Cellular Probes|October 1, 1996
A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intoleranceR Dumoulin, I Sagnol, T Ferlin, et al.Biochimica Et Biophysica Acta|June 13, 1998
COS cell expression studies of P86L, P86R, P480L and P480Q Hunter's disease-causing mutationsG Millat, R Froissart, S Cudry, et al.FEBS Letters|June 16, 2000
Creatine kinase isoenzymes specificities: histidine 65 in human CK-BB, a role in protein stability, not in catalysisT Mourad-Terzian, J P Steghens, K L Min, et al.American Journal of Human Genetics|June 1, 1992
Genetic determination of exocrine pancreatic function in cystic fibrosisP Kristidis, D Bozon, M Corey, et al.Journal of Medical Genetics|July 1, 1994
Mutation analysis in 600 French cystic fibrosis patientsF Chevalier-Porst, A M Bonardot, R Gilly, et al.Human Molecular Genetics|June 1, 1993
Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621 + 1G-->T and 711 + 1G-->T mutationsJ Zielenski, D Bozon, D Markiewicz, et al.Journal of Medical Genetics|May 1, 1996
Mutation analysis in 24 French patients with glycogen storage disease type 1aF Chevalier-Porst, D Bozon, A M Bonardot, et al.Pageof 4