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C Dodé

Showing results (11-20 of 35) with videos related to

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Human Genetics|August 1, 1989
Autosomal dominant polycystic kidney disease and alpha -4.2 thalassemia in a Caucasian familyM C Vinet, C Dodé, O Pascal, et al.
Clinical and Experimental Rheumatology|November 14, 2007
Overlap syndrome between FMF and TRAPS in a patient carrying MEFV and TNFRSF1A mutationsB Granel, J Serratrice, C Dodé, et al.
Kidney International|April 25, 2001
Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid CommunicationM Jadoul, C Dodé, J P Cosyns, et al.
Annals of the Rheumatic Diseases|March 30, 2006
Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A geneN Ravet, S Rouaghe, C Dodé, et al.
Genomics|February 18, 1998
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2)C Dodé, D Weil, J Levilliers, et al.
American Journal of Medical Genetics|June 8, 2000
Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean feverC Dodé, C Pêcheux, C Cazeneuve, et al.
QJM : Monthly Journal of the Association of Physicians|April 29, 2000
Clinical versus genetic diagnosis of familial Mediterranean feverG Grateau, C Pêcheux, C Cazeneuve, et al.
Journal of Medical Genetics|May 1, 1995
Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomesC Pêcheux, J F Mouret, A Dürr, et al.
Journal of the Neurological Sciences|March 1, 1995
Diagnosis of "sporadic" Huntington's diseaseA Dürr, C Dodé, V Hahn, et al.
Human Molecular Genetics|July 1, 1996
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22H Chaib, C Place, N Salem, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Human Genetics|August 1, 1989
Autosomal dominant polycystic kidney disease and alpha -4.2 thalassemia in a Caucasian familyM C Vinet, C Dodé, O Pascal, et al.
Clinical and Experimental Rheumatology|November 14, 2007
Overlap syndrome between FMF and TRAPS in a patient carrying MEFV and TNFRSF1A mutationsB Granel, J Serratrice, C Dodé, et al.
Kidney International|April 25, 2001
Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid CommunicationM Jadoul, C Dodé, J P Cosyns, et al.
Annals of the Rheumatic Diseases|March 30, 2006
Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A geneN Ravet, S Rouaghe, C Dodé, et al.
Genomics|February 18, 1998
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2)C Dodé, D Weil, J Levilliers, et al.
American Journal of Medical Genetics|June 8, 2000
Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean feverC Dodé, C Pêcheux, C Cazeneuve, et al.
QJM : Monthly Journal of the Association of Physicians|April 29, 2000
Clinical versus genetic diagnosis of familial Mediterranean feverG Grateau, C Pêcheux, C Cazeneuve, et al.
Journal of Medical Genetics|May 1, 1995
Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomesC Pêcheux, J F Mouret, A Dürr, et al.
Journal of the Neurological Sciences|March 1, 1995
Diagnosis of "sporadic" Huntington's diseaseA Dürr, C Dodé, V Hahn, et al.
Human Molecular Genetics|July 1, 1996
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22H Chaib, C Place, N Salem, et al.
Pageof 4