M P Audrezet - JoVE Visualize

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Pathologie-Biologie|October 14, 1998

TP53 and oesophageal cancerC Ferec, M A Giroux, M P Audrezet, et al.

Nature Genetics|June 1, 1992

Detection of over 98% cystic fibrosis mutations in a Celtic populationC Férec, M P Audrezet, B Mercier, 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.

Prenatal Diagnosis|December 1, 1993

Asymptomatic carrier of two CFTR mutations: consequences for prenatal diagnosis?C Verlingue, A David, M P Audrezet, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

Autosomal dominant polycystic kidney disease in University Clinic of Nephrology and Haemodialysis of Cotonou: clinical and genetical findingsA Laleye, B Awede, B Agboton, et al.

Genetic Counseling (Geneva, Switzerland)|March 23, 2007

Prenatal diagnosis of a mosaic 45,X/46,X,r(X)46,XX with a small ring of the X chromosomeM J Le Bris, H Le Guern, C Plouhinec, et al.

Biochimica Et Biophysica Acta|May 30, 1998

Transgene expression kinetics after transfection with cationic phosphonolipids in hematopoietic non adherent cellsV Floch, M P Audrezet, C Guillaume, et al.

Journal of Inherited Metabolic Disease|July 17, 2007

Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutationsM Roussey, A Le Bihannic, V Scotet, et al.

Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 25, 2022

The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapyA Bergougnoux, A Billet, C Ka, et al.

Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:

Pageof 1

Pathologie-Biologie|October 14, 1998

TP53 and oesophageal cancerC Ferec, M A Giroux, M P Audrezet, et al.

Nature Genetics|June 1, 1992

Detection of over 98% cystic fibrosis mutations in a Celtic populationC Férec, M P Audrezet, B Mercier, 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.

Prenatal Diagnosis|December 1, 1993

Asymptomatic carrier of two CFTR mutations: consequences for prenatal diagnosis?C Verlingue, A David, M P Audrezet, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

Autosomal dominant polycystic kidney disease in University Clinic of Nephrology and Haemodialysis of Cotonou: clinical and genetical findingsA Laleye, B Awede, B Agboton, et al.

Genetic Counseling (Geneva, Switzerland)|March 23, 2007

Prenatal diagnosis of a mosaic 45,X/46,X,r(X)46,XX with a small ring of the X chromosomeM J Le Bris, H Le Guern, C Plouhinec, et al.

Biochimica Et Biophysica Acta|May 30, 1998

Transgene expression kinetics after transfection with cationic phosphonolipids in hematopoietic non adherent cellsV Floch, M P Audrezet, C Guillaume, et al.

Journal of Inherited Metabolic Disease|July 17, 2007

Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutationsM Roussey, A Le Bihannic, V Scotet, et al.

Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 25, 2022

The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapyA Bergougnoux, A Billet, C Ka, et al.

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