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B Arveiler

Showing results (21-30 of 64) with videos related to

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Clinical and Experimental Rheumatology|June 21, 2008
Influence of FCGR3A-V212F and TNFRSF1B-M196R genotypes in patients with rheumatoid arthritis treated with infliximab therapyC Rooryck, T Barnetche, C Richez, et al.
European Journal of Dermatology : EJD|November 10, 2001
Familial aggregation of vitiligo in the French West Indies (Isle of Martinique)A M Boisseau-Garsaud, I Saint-Cyr, D Quist, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndromeA Bloch-Zupan, J Stachtou, D Emmanouil, et al.
Gene|May 23, 1998
A new yeast artificial chromosome vector designed for gene transfer into mammalian cellsP J Ripoll, A Cowper, S Salmeron, et al.
Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
American Journal of Human Genetics|May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndromeB Arveiler, G de Saint-Basile, A Fischer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 24, 2017
ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patientJ Petre, E Lasseaux, C Ged, et al.
American Journal of Medical Genetics|May 1, 1988
Improved DNA markers for efficient analysis of fragile X familiesR Heilig, I Oberlé, B Arveiler, et al.
Nucleic Acids Research|February 25, 1987
RFLPs for the human erythrocyte membrane glycophorin C geneB Arveiler, C Le Van Kim, Y Colin, et al.
Clinical and Experimental Dermatology|February 23, 2020
Lentiginosis and café-au-lait macules as part of the phenotypic spectrum of PAX3-related disordersF Morice-Picard, O Letertre, E Lasseaux, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
Clinical and Experimental Rheumatology|June 21, 2008
Influence of FCGR3A-V212F and TNFRSF1B-M196R genotypes in patients with rheumatoid arthritis treated with infliximab therapyC Rooryck, T Barnetche, C Richez, et al.
European Journal of Dermatology : EJD|November 10, 2001
Familial aggregation of vitiligo in the French West Indies (Isle of Martinique)A M Boisseau-Garsaud, I Saint-Cyr, D Quist, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndromeA Bloch-Zupan, J Stachtou, D Emmanouil, et al.
Gene|May 23, 1998
A new yeast artificial chromosome vector designed for gene transfer into mammalian cellsP J Ripoll, A Cowper, S Salmeron, et al.
Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
American Journal of Human Genetics|May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndromeB Arveiler, G de Saint-Basile, A Fischer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 24, 2017
ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patientJ Petre, E Lasseaux, C Ged, et al.
American Journal of Medical Genetics|May 1, 1988
Improved DNA markers for efficient analysis of fragile X familiesR Heilig, I Oberlé, B Arveiler, et al.
Nucleic Acids Research|February 25, 1987
RFLPs for the human erythrocyte membrane glycophorin C geneB Arveiler, C Le Van Kim, Y Colin, et al.
Clinical and Experimental Dermatology|February 23, 2020
Lentiginosis and café-au-lait macules as part of the phenotypic spectrum of PAX3-related disordersF Morice-Picard, O Letertre, E Lasseaux, et al.
Pageof 7