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L Villard

Showing results (61-70 of 99) with videos related to

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Nature Genetics|April 1, 1996
XNP mutation in a large family with Juberg-Marsidi syndromeL Villard, J Gecz, J F Mattéi, et al.
Human Molecular Genetics|January 1, 1994
Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3J Gecz, H Pollard, G Consalez, et al.
Zentralblatt Fur Veterinarmedizin. Reihe B. Journal of Veterinary Medicine. Series B|February 19, 1998
Isolation and identification of Salmonella species from chelonians using combined selective media, serotyping and ribotypingA Kodjo, L Villard, M Prave, et al.
Hormone Research|September 29, 2004
Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?K M Lower, R Kumar, E Woollatt, et al.
Physical Review Letters|January 15, 2011
System size effects on gyrokinetic turbulenceB F McMillan, X Lapillonne, S Brunner, et al.
Genomics|July 15, 1997
Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicaseL Villard, A M Lossi, C Cardoso, et al.
American Journal of Human Genetics|July 27, 1999
Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation biasA M Lossi, J M Millán, L Villard, et al.
Veterinary Journal (London, England : 1997)|April 21, 2006
Serological and molecular comparison of Mannheimia haemolytica and Pasteurella trehalosi strains isolated from wild and domestic ruminants in the French AlpsL Villard, D Gauthier, A Lacheretz, et al.
Nucleic Acids Symposium Series (2004)|September 9, 2008
A step further in the SATE mononucleotide prodrug approachS Peyrottes, A-L Villard, G Coussot, et al.
Journal of Medical Genetics|June 17, 2003
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasiaN Philip, B Chabrol, A-M Lossi, et al.
Pageof 10

Showing results (61-70 of 99) with videos related to

Sort By:
Pageof 10
Nature Genetics|April 1, 1996
XNP mutation in a large family with Juberg-Marsidi syndromeL Villard, J Gecz, J F Mattéi, et al.
Human Molecular Genetics|January 1, 1994
Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3J Gecz, H Pollard, G Consalez, et al.
Zentralblatt Fur Veterinarmedizin. Reihe B. Journal of Veterinary Medicine. Series B|February 19, 1998
Isolation and identification of Salmonella species from chelonians using combined selective media, serotyping and ribotypingA Kodjo, L Villard, M Prave, et al.
Hormone Research|September 29, 2004
Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?K M Lower, R Kumar, E Woollatt, et al.
Physical Review Letters|January 15, 2011
System size effects on gyrokinetic turbulenceB F McMillan, X Lapillonne, S Brunner, et al.
Genomics|July 15, 1997
Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicaseL Villard, A M Lossi, C Cardoso, et al.
American Journal of Human Genetics|July 27, 1999
Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation biasA M Lossi, J M Millán, L Villard, et al.
Veterinary Journal (London, England : 1997)|April 21, 2006
Serological and molecular comparison of Mannheimia haemolytica and Pasteurella trehalosi strains isolated from wild and domestic ruminants in the French AlpsL Villard, D Gauthier, A Lacheretz, et al.
Nucleic Acids Symposium Series (2004)|September 9, 2008
A step further in the SATE mononucleotide prodrug approachS Peyrottes, A-L Villard, G Coussot, et al.
Journal of Medical Genetics|June 17, 2003
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasiaN Philip, B Chabrol, A-M Lossi, et al.
Pageof 10