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D Vidaud

Showing results (41-50 of 70) with videos related to

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Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|December 1, 1994
Three novel mutations of antithrombin inducing high-molecular-mass compoundsJ Emmerich, D Vidaud, M Alhenc-Gelas, et al.
Annales De Genetique|September 22, 2000
Human TIP49b/RUVBL2 gene: genomic structure, expression pattern, physical link to the human CGB/LHB gene cluster on chromosome 19q13.3B Parfait, Y Giovangrandi, M Asheuer, et al.
Journal of Medical Genetics|September 22, 2001
GDNF as a candidate modifier in a type 1 neurofibromatosis (NF1) enteric phenotypeM Bahuau, A Pelet, D Vidaud, et al.
Human Genetics|December 1, 1996
Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patientsC Lázaro, A Gaona, P Ainsworth, et al.
Gut|October 18, 2005
Plexiform neurofibroma mimicking a pancreatic cystic tumourA Handra-Luca, D Vidaud, M-P Vullierme, et al.
Journal of Molecular Biology|April 9, 2001
A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definitionL J Fang, M J Simard, D Vidaud, et al.
American Journal of Human Genetics|July 1, 1988
Determination of the spectrum of beta-thalassemia genes in Spain by use of dot-blot analysis of amplified beta-globin DNAS Amselem, V Nunes, M Vidaud, et al.
Neuro-Chirurgie|June 16, 2015
Neurofibromatosis type 2 French cohort analysis using a comprehensive NF2 molecular diagnostic strategyE Pasmant, C Louvrier, A Luscan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 6, 2017
[Type 1 neurofibromatosis: Onset of two tumors before the age of 5years]M Remillieux, C Durand, H Sartelet, et al.
British Journal of Haematology|July 1, 1991
Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VIS Gandrille, D Vidaud, J Emmerich, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|December 1, 1994
Three novel mutations of antithrombin inducing high-molecular-mass compoundsJ Emmerich, D Vidaud, M Alhenc-Gelas, et al.
Annales De Genetique|September 22, 2000
Human TIP49b/RUVBL2 gene: genomic structure, expression pattern, physical link to the human CGB/LHB gene cluster on chromosome 19q13.3B Parfait, Y Giovangrandi, M Asheuer, et al.
Journal of Medical Genetics|September 22, 2001
GDNF as a candidate modifier in a type 1 neurofibromatosis (NF1) enteric phenotypeM Bahuau, A Pelet, D Vidaud, et al.
Human Genetics|December 1, 1996
Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patientsC Lázaro, A Gaona, P Ainsworth, et al.
Gut|October 18, 2005
Plexiform neurofibroma mimicking a pancreatic cystic tumourA Handra-Luca, D Vidaud, M-P Vullierme, et al.
Journal of Molecular Biology|April 9, 2001
A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definitionL J Fang, M J Simard, D Vidaud, et al.
American Journal of Human Genetics|July 1, 1988
Determination of the spectrum of beta-thalassemia genes in Spain by use of dot-blot analysis of amplified beta-globin DNAS Amselem, V Nunes, M Vidaud, et al.
Neuro-Chirurgie|June 16, 2015
Neurofibromatosis type 2 French cohort analysis using a comprehensive NF2 molecular diagnostic strategyE Pasmant, C Louvrier, A Luscan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 6, 2017
[Type 1 neurofibromatosis: Onset of two tumors before the age of 5years]M Remillieux, C Durand, H Sartelet, et al.
British Journal of Haematology|July 1, 1991
Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VIS Gandrille, D Vidaud, J Emmerich, et al.
Pageof 7