N Ghanem|E Girodon|M Vidaud|J Martin|P Fanen|F Plassa|M Goossens - JoVE Visualize

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Human Mutation|January 1, 1992

A comprehensive scanning method for rapid detection of beta-globin gene mutations and polymorphismsN Ghanem, E Girodon, M Vidaud, et al.

Genomics|July 1, 1992

Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctionsP Fanen, N Ghanem, M Vidaud, et al.

Molecular and Cellular Probes|April 1, 1993

Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemiasN Ghanem, M Vidaud, F Plassa, et al.

Genomics|May 15, 1994

Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) geneN Ghanem, B Costes, E Girodon, et al.

Human Genetics|September 1, 1990

Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresisM Vidaud, P Fanen, J Martin, et al.

Revue De Pneumologie Clinique|January 1, 1995

[Cystic fibrosis: the CFTR gene, its mutations, the genetic counseling]M Goossens, N Ghanem, E Girodon, et al.

Annals of Hematology|October 1, 1992

Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variantsE Girodon, N Ghanem, M Vidaud, et al.

Molecular and Cellular Probes|February 1, 1992

Exhaustive screening of exon 10 CFTR gene mutations and polymorphisms by denaturing gradient gel electrophoresis: applications to genetic counselling in cystic fibrosisN Ghanem, P Fanen, J Martin, et al.

Journal of the International Federation of Clinical Chemistry|March 9, 1995

Prenatal diagnosis of hemoglobinopathiesE Girodon, N Ghanem, M Goossens

Human Mutation|April 17, 1999

Identification of cystic fibrosis mutations in the United Arab Emirates. Mutations in brief no. 133. OnlineP M Frossard, E Girodon, K P Dawson, et al.

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Showing results (1-10 of 10,430) with videos related to

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Pageof 1,043

Human Mutation|January 1, 1992

A comprehensive scanning method for rapid detection of beta-globin gene mutations and polymorphismsN Ghanem, E Girodon, M Vidaud, et al.

Genomics|July 1, 1992

Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctionsP Fanen, N Ghanem, M Vidaud, et al.

Molecular and Cellular Probes|April 1, 1993

Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemiasN Ghanem, M Vidaud, F Plassa, et al.

Genomics|May 15, 1994

Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) geneN Ghanem, B Costes, E Girodon, et al.

Human Genetics|September 1, 1990

Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresisM Vidaud, P Fanen, J Martin, et al.

Revue De Pneumologie Clinique|January 1, 1995

[Cystic fibrosis: the CFTR gene, its mutations, the genetic counseling]M Goossens, N Ghanem, E Girodon, et al.

Annals of Hematology|October 1, 1992

Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variantsE Girodon, N Ghanem, M Vidaud, et al.

Molecular and Cellular Probes|February 1, 1992

Exhaustive screening of exon 10 CFTR gene mutations and polymorphisms by denaturing gradient gel electrophoresis: applications to genetic counselling in cystic fibrosisN Ghanem, P Fanen, J Martin, et al.

Journal of the International Federation of Clinical Chemistry|March 9, 1995

Prenatal diagnosis of hemoglobinopathiesE Girodon, N Ghanem, M Goossens

Human Mutation|April 17, 1999

Identification of cystic fibrosis mutations in the United Arab Emirates. Mutations in brief no. 133. OnlineP M Frossard, E Girodon, K P Dawson, et al.

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