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D Vidaud

Showing results (1-10 of 70) with videos related to

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Annales De Dermatologie Et De Venereologie|October 11, 2007
[NF1: Molecular testing in clinical practice]C Rieubland, D Vidaud, S Jacquemont
Archives Francaises De Pediatrie|May 1, 1988
[Hereditary persistence of fetal hemoglobin associated with mutation above the gamma gene]D Vidaud-Raphanaud, J Badoual, D Labie
Annales De Genetique|January 1, 1988
Interaction of deletional alpha-thalassaemia with sickle cell beta-thalassaemia and its influence on foetal haemoglobin expressionD Vidaud-Raphanaud, R Krishnamoorthy, G Schaison, et al.
Annales De Genetique|January 1, 1987
[Analysis of the recombination zone in hereditary persistence of fetal hemoglobin with fetal gene rearrangement of the G gamma-G gamma-A gamma type]D Vidaud-Raphanaud, E Bouhassira, D Labie, et al.
Human Mutation|December 19, 2001
Identification and characterization of four novel large deletions in the human neurofibromatosis type 1 (NF1) geneL J Fang, D Vidaud, M Vidaud, et al.
Molecular and Biochemical Parasitology|June 1, 1991
Structure of the Echinococcus multilocularis U1 snRNA gene repeatS Bretagne, B Robert, D Vidaud, et al.
Thyroid : Official Journal of the American Thyroid Association|April 6, 2001
Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reactionI Bièche, B Franc, D Vidaud, et al.
Experimental Parasitology|April 1, 1996
Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genesS Bretagne, B Assouline, D Vidaud, et al.
Neurology|May 1, 1996
Misdiagnosis revealed by genetic linkage analysis in a family with Wilson diseaseD Vidaud, B Assouline, P Lecoz, et al.
Annales De Dermatologie Et De Venereologie|February 22, 2011
[McCune-Albright syndrome]A Saussine, L Valeyrie-Allanore, D Vidaud, et al.
Pageof 7

Showing results (1-10 of 70) with videos related to

Sort By:
Pageof 7
Annales De Dermatologie Et De Venereologie|October 11, 2007
[NF1: Molecular testing in clinical practice]C Rieubland, D Vidaud, S Jacquemont
Archives Francaises De Pediatrie|May 1, 1988
[Hereditary persistence of fetal hemoglobin associated with mutation above the gamma gene]D Vidaud-Raphanaud, J Badoual, D Labie
Annales De Genetique|January 1, 1988
Interaction of deletional alpha-thalassaemia with sickle cell beta-thalassaemia and its influence on foetal haemoglobin expressionD Vidaud-Raphanaud, R Krishnamoorthy, G Schaison, et al.
Annales De Genetique|January 1, 1987
[Analysis of the recombination zone in hereditary persistence of fetal hemoglobin with fetal gene rearrangement of the G gamma-G gamma-A gamma type]D Vidaud-Raphanaud, E Bouhassira, D Labie, et al.
Human Mutation|December 19, 2001
Identification and characterization of four novel large deletions in the human neurofibromatosis type 1 (NF1) geneL J Fang, D Vidaud, M Vidaud, et al.
Molecular and Biochemical Parasitology|June 1, 1991
Structure of the Echinococcus multilocularis U1 snRNA gene repeatS Bretagne, B Robert, D Vidaud, et al.
Thyroid : Official Journal of the American Thyroid Association|April 6, 2001
Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reactionI Bièche, B Franc, D Vidaud, et al.
Experimental Parasitology|April 1, 1996
Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genesS Bretagne, B Assouline, D Vidaud, et al.
Neurology|May 1, 1996
Misdiagnosis revealed by genetic linkage analysis in a family with Wilson diseaseD Vidaud, B Assouline, P Lecoz, et al.
Annales De Dermatologie Et De Venereologie|February 22, 2011
[McCune-Albright syndrome]A Saussine, L Valeyrie-Allanore, D Vidaud, et al.
Pageof 7