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Human Mutation
|
December 29, 1999
UMD (Universal mutation database): a generic software to build and analyze locus-specific databases
C 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 gene
M 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 mutation
G 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 gene
G 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 software
G Collod-Béroud, C Béroud, L Ades, et al.
Journal of Medical Genetics
|
March 31, 2006
The molecular genetics of Marfan syndrome and related disorders
P N Robinson, E Arteaga-Solis, C Baldock, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Human Mutation
|
December 29, 1999
UMD (Universal mutation database): a generic software to build and analyze locus-specific databases
C 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 gene
M 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 mutation
G 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 gene
G 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 software
G Collod-Béroud, C Béroud, L Ades, et al.
Journal of Medical Genetics
|
March 31, 2006
The molecular genetics of Marfan syndrome and related disorders
P N Robinson, E Arteaga-Solis, C Baldock, et al.
Page
of 1