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G Collod-Béroud

Showing results (1-10 of 8) with videos related to

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Human Mutation|December 29, 1999
UMD (Universal mutation database): a generic software to build and analyze locus-specific databasesC Béroud, G Collod-Béroud, C Boileau, et al.
Revue Neurologique|October 20, 2009
[Monogenetic dystonia: revisiting the dopaminergic hypothesis]A Blanchard, A Roubertie, M Y Frédéric, et al.
Nucleic Acids Research|January 1, 1997
Software and database for the analysis of mutations in the human LDL receptor geneM Varret, J P Rabès, G Collod-Béroud, et al.
American Journal of Human Genetics|August 12, 1999
Demonstration of the recurrence of Marfan-like skeletal and cardiovascular manifestations due to germline mosaicism for an FBN1 mutationG Collod-Béroud, M Lackmy-Port-Lys, G Jondeau, et al.
Nucleic Acids Research|January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 geneG Collod-Béroud, C Béroud, L Adès, et al.
Pathologie-Biologie|December 4, 2009
[Genetic mutation databases: stakes and perspectives for orphan genetic diseases]V Humbertclaude, S Tuffery-Giraud, C Bareil, et al.
Nucleic Acids Research|February 21, 1998
Marfan Database (third edition): new mutations and new routines for the softwareG Collod-Béroud, C Béroud, L Ades, et al.
Journal of Medical Genetics|March 31, 2006
The molecular genetics of Marfan syndrome and related disordersP N Robinson, E Arteaga-Solis, C Baldock, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Human Mutation|December 29, 1999
UMD (Universal mutation database): a generic software to build and analyze locus-specific databasesC Béroud, G Collod-Béroud, C Boileau, et al.
Revue Neurologique|October 20, 2009
[Monogenetic dystonia: revisiting the dopaminergic hypothesis]A Blanchard, A Roubertie, M Y Frédéric, et al.
Nucleic Acids Research|January 1, 1997
Software and database for the analysis of mutations in the human LDL receptor geneM Varret, J P Rabès, G Collod-Béroud, et al.
American Journal of Human Genetics|August 12, 1999
Demonstration of the recurrence of Marfan-like skeletal and cardiovascular manifestations due to germline mosaicism for an FBN1 mutationG Collod-Béroud, M Lackmy-Port-Lys, G Jondeau, et al.
Nucleic Acids Research|January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 geneG Collod-Béroud, C Béroud, L Adès, et al.
Pathologie-Biologie|December 4, 2009
[Genetic mutation databases: stakes and perspectives for orphan genetic diseases]V Humbertclaude, S Tuffery-Giraud, C Bareil, et al.
Nucleic Acids Research|February 21, 1998
Marfan Database (third edition): new mutations and new routines for the softwareG Collod-Béroud, C Béroud, L Ades, et al.
Journal of Medical Genetics|March 31, 2006
The molecular genetics of Marfan syndrome and related disordersP N Robinson, E Arteaga-Solis, C Baldock, et al.
Pageof 1