O Raguenes - JoVE Visualize

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Blood|April 9, 1999

HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosisC Mura, O Raguenes, C Férec

Fetal Diagnosis and Therapy|September 1, 1993

Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresisC Férec, C Verlingue, M P Audrézet, et al.

Blood Cells, Molecules & Diseases|October 24, 2000

Nramp2 analysis in hemochromatosis probandsG Le Gac, C Mura, O Raguenes, et al.

Human Genetics|January 24, 1998

Phenotype-genotype correlation in haemochromatosis subjectsC Mura, J B Nousbaum, P Verger, et al.

Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|October 28, 1998

[The hemochromatosis gene (HFE). Molecular analysis--diagnostic applications]C Ferec, O Raguenes, A Y Mercier, et al.

Blood Cells, Molecules & Diseases|April 25, 2000

Clinical and molecular aspects of juvenile hemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, canada)S R Rivard, C Mura, H Simard, et al.

British Journal of Haematology|May 3, 2000

Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada)S R Rivard, C Mura, H Simard, et al.

European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|April 1, 1994

HLA-DRB and -DBQ typing by PCR amplification using sequence-specific primers (PCR-SSP): assessment after 1 year of routine use by three laboratoriesB Mercier, R al Daccak, A Samaan, et al.

Human Heredity|January 1, 1995

Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patientsS M Cashman, A Patino, A Martinez, et al.

Clinical Genetics|March 22, 2001

Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitisJ M Chen, A Piepoli Bis, L Le Bodic, et al.

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

Sort By:

Pageof 1

Blood|April 9, 1999

HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosisC Mura, O Raguenes, C Férec

Fetal Diagnosis and Therapy|September 1, 1993

Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresisC Férec, C Verlingue, M P Audrézet, et al.

Blood Cells, Molecules & Diseases|October 24, 2000

Nramp2 analysis in hemochromatosis probandsG Le Gac, C Mura, O Raguenes, et al.

Human Genetics|January 24, 1998

Phenotype-genotype correlation in haemochromatosis subjectsC Mura, J B Nousbaum, P Verger, et al.

Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|October 28, 1998

[The hemochromatosis gene (HFE). Molecular analysis--diagnostic applications]C Ferec, O Raguenes, A Y Mercier, et al.

Blood Cells, Molecules & Diseases|April 25, 2000

Clinical and molecular aspects of juvenile hemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, canada)S R Rivard, C Mura, H Simard, et al.

British Journal of Haematology|May 3, 2000

Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada)S R Rivard, C Mura, H Simard, et al.

European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|April 1, 1994

HLA-DRB and -DBQ typing by PCR amplification using sequence-specific primers (PCR-SSP): assessment after 1 year of routine use by three laboratoriesB Mercier, R al Daccak, A Samaan, et al.

Human Heredity|January 1, 1995

Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patientsS M Cashman, A Patino, A Martinez, et al.

Clinical Genetics|March 22, 2001

Mutational screening of the cationic trypsinogen gene in a large cohort of subjects with idiopathic chronic pancreatitisJ M Chen, A Piepoli Bis, L Le Bodic, et al.

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