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B Mercier

Showing results (101-110 of 164) with videos related to

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European Journal of Human Genetics : EJHG|June 15, 2000
Novel mutations in the duplicated region of PKD1 geneR Perrichot, B Mercier, I Quere, et al.
Human Mutation|January 1, 1997
Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in the CFTR geneM Macek, B Mercier, A Macková, et al.
Human Mutation|January 1, 1995
Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delTB Mercier, W Lissens, M P Audrézet, et al.
Journal of Medical Genetics|May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTRW Lissens, S Desmyttere, M Bonduelle, et al.
European Journal of Applied Physiology and Occupational Physiology|July 11, 1998
Noninvasive skeletal muscle lactate detection between periods of intense exercise in humansB Mercier, P Granier, J Mercier, et al.
Human Mutation|January 1, 1994
Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->AB Mercier, M P Audrézet, J Feigelson, et al.
Human Mutation|January 1, 1995
Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel allelesC Verlingue, N I Kapranov, B Mercier, et al.
American Journal of Human Genetics|January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patientsB Mercier, C Verlingue, W Lissens, et al.
Thrombosis and Haemostasis|July 15, 2000
Prevalence of factor V Leiden in patients with myocardial infarction and normal coronary angiographyJ Mansourati, A Da Costa, S Munier, et al.
Journal of Neurology|March 1, 1992
Lymphoma-induced polyradiculopathy in AIDS: two casesJ M Léger, D Hénin, L Bélec, et al.
Pageof 17

Showing results (101-110 of 164) with videos related to

Sort By:
Pageof 17
European Journal of Human Genetics : EJHG|June 15, 2000
Novel mutations in the duplicated region of PKD1 geneR Perrichot, B Mercier, I Quere, et al.
Human Mutation|January 1, 1997
Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in the CFTR geneM Macek, B Mercier, A Macková, et al.
Human Mutation|January 1, 1995
Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delTB Mercier, W Lissens, M P Audrézet, et al.
Journal of Medical Genetics|May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTRW Lissens, S Desmyttere, M Bonduelle, et al.
European Journal of Applied Physiology and Occupational Physiology|July 11, 1998
Noninvasive skeletal muscle lactate detection between periods of intense exercise in humansB Mercier, P Granier, J Mercier, et al.
Human Mutation|January 1, 1994
Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->AB Mercier, M P Audrézet, J Feigelson, et al.
Human Mutation|January 1, 1995
Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel allelesC Verlingue, N I Kapranov, B Mercier, et al.
American Journal of Human Genetics|January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patientsB Mercier, C Verlingue, W Lissens, et al.
Thrombosis and Haemostasis|July 15, 2000
Prevalence of factor V Leiden in patients with myocardial infarction and normal coronary angiographyJ Mansourati, A Da Costa, S Munier, et al.
Journal of Neurology|March 1, 1992
Lymphoma-induced polyradiculopathy in AIDS: two casesJ M Léger, D Hénin, L Bélec, et al.
Pageof 17