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American Journal of Medical Genetics
|
October 26, 2000
Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families
A M Lossi, L Colleaux, P Chiaroni, et al.
Journal of Clinical Microbiology
|
January 16, 1999
Pulsed-field gel electrophoresis is more efficient than ribotyping and random amplified polymorphic DNA analysis in discrimination of Pasteurella haemolytica strains
A Kodjo, L Villard, C Bizet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature review
M-V André, P Cacciagli, A Cano, et al.
Genomics
|
March 1, 1995
Construction of a YAC contig spanning the Xq13.3 subband
L Villard, J Gecz, L Colleaux, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
June 30, 2006
Diastereoisomeric resolution of a pronucleotide using solid phase extraction and high performance liquid chromatography: application to a stereoselective decomposition kinetic in cell extracts
C Foulon, C Vaccher, A-L Villard, et al.
Biomedical Chromatography : BMC
|
July 23, 2005
Column selection and method development for the separation of nucleoside phosphotriester diastereoisomers, new potential anti-viral drugs. Application to cellular extract analysis
J F Goossens, C Foulon, A-L Villard, et al.
Letters in Applied Microbiology
|
April 4, 2000
Detection of Escherichia coli O157:H7 in heifers' faecal samples using an automated immunoconcentration system
C Vernozy-Rozand, P Feng, M P Montet, et al.
Journal of Medical Genetics
|
October 7, 2004
Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males
V Cantagrel, A-M Lossi, S Boulanger, et al.
Journal of Medical Genetics
|
February 12, 2002
Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation
A M Lossi, F Laugier-Anfossi, D Depetris, et al.
American Journal of Medical Genetics
|
July 12, 1996
X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1
M Raynaud, C Gendrot, B Dessay, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 99) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics
|
October 26, 2000
Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families
A M Lossi, L Colleaux, P Chiaroni, et al.
Journal of Clinical Microbiology
|
January 16, 1999
Pulsed-field gel electrophoresis is more efficient than ribotyping and random amplified polymorphic DNA analysis in discrimination of Pasteurella haemolytica strains
A Kodjo, L Villard, C Bizet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature review
M-V André, P Cacciagli, A Cano, et al.
Genomics
|
March 1, 1995
Construction of a YAC contig spanning the Xq13.3 subband
L Villard, J Gecz, L Colleaux, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
June 30, 2006
Diastereoisomeric resolution of a pronucleotide using solid phase extraction and high performance liquid chromatography: application to a stereoselective decomposition kinetic in cell extracts
C Foulon, C Vaccher, A-L Villard, et al.
Biomedical Chromatography : BMC
|
July 23, 2005
Column selection and method development for the separation of nucleoside phosphotriester diastereoisomers, new potential anti-viral drugs. Application to cellular extract analysis
J F Goossens, C Foulon, A-L Villard, et al.
Letters in Applied Microbiology
|
April 4, 2000
Detection of Escherichia coli O157:H7 in heifers' faecal samples using an automated immunoconcentration system
C Vernozy-Rozand, P Feng, M P Montet, et al.
Journal of Medical Genetics
|
October 7, 2004
Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males
V Cantagrel, A-M Lossi, S Boulanger, et al.
Journal of Medical Genetics
|
February 12, 2002
Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation
A M Lossi, F Laugier-Anfossi, D Depetris, et al.
American Journal of Medical Genetics
|
July 12, 1996
X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1
M Raynaud, C Gendrot, B Dessay, et al.
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of 10