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G Lucotte

Showing results (111-120 of 199) with videos related to

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Molecular and Cellular Probes|February 13, 2001
PCR test for diagnosis of the common GJB2 (connexin 26) 35delG mutation on dried blood spots and determination of the carrier frequency in FranceG Lucotte, C Bathelier, T Champenois
Experimental and Clinical Immunogenetics|January 1, 1988
Correlation of class I DNA TaqI and PvuII restriction HLA gene fragments with serologic HLA-C allelesM Mariotti, F David, G Lucotte
Experimental and Clinical Immunogenetics|January 1, 1985
Correlation of class I DNA Pvu II restriction HLA gene fragments with serologic allelesG Lucotte, C Coulondre, C Salmon
Annals of Neurology|September 11, 1999
Acetylator genotype for N-acetyltransferase 2 and Parkinson's diseaseJ M Dupret, S Longuemaux, G Lucotte
Nucleic Acids Research|January 12, 1987
Two Taq I RFLPs for human alpha-2 macroglobulin (alpha 2M) using a full length cDNA probeF David, C C Kan, G Lucotte
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1991
The p49/TaqI Y-specific DNA haplotypes in Australian aboriginesG Lucotte, S Hazout, K M Summers
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 21, 1999
Chromosome 19 locus apolipoprotein C-II association with multiple sclerosisH Zouali, L Faure-Delanef, G Lucotte
Journal of Neurology, Neurosurgery, and Psychiatry|December 17, 1998
Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's diseaseG Lucotte, G Mercier, J C Turpin
Journal of Neurology|February 13, 1999
Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association foundG Mercier, J C Turpin, G Lucotte
Human Genetics|April 1, 1993
A recombinant Friedreich's ataxia familyG Lucotte, S Berriche, J C Turpin
Pageof 20

Showing results (111-120 of 199) with videos related to

Sort By:
Pageof 20
Molecular and Cellular Probes|February 13, 2001
PCR test for diagnosis of the common GJB2 (connexin 26) 35delG mutation on dried blood spots and determination of the carrier frequency in FranceG Lucotte, C Bathelier, T Champenois
Experimental and Clinical Immunogenetics|January 1, 1988
Correlation of class I DNA TaqI and PvuII restriction HLA gene fragments with serologic HLA-C allelesM Mariotti, F David, G Lucotte
Experimental and Clinical Immunogenetics|January 1, 1985
Correlation of class I DNA Pvu II restriction HLA gene fragments with serologic allelesG Lucotte, C Coulondre, C Salmon
Annals of Neurology|September 11, 1999
Acetylator genotype for N-acetyltransferase 2 and Parkinson's diseaseJ M Dupret, S Longuemaux, G Lucotte
Nucleic Acids Research|January 12, 1987
Two Taq I RFLPs for human alpha-2 macroglobulin (alpha 2M) using a full length cDNA probeF David, C C Kan, G Lucotte
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1991
The p49/TaqI Y-specific DNA haplotypes in Australian aboriginesG Lucotte, S Hazout, K M Summers
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 21, 1999
Chromosome 19 locus apolipoprotein C-II association with multiple sclerosisH Zouali, L Faure-Delanef, G Lucotte
Journal of Neurology, Neurosurgery, and Psychiatry|December 17, 1998
Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's diseaseG Lucotte, G Mercier, J C Turpin
Journal of Neurology|February 13, 1999
Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association foundG Mercier, J C Turpin, G Lucotte
Human Genetics|April 1, 1993
A recombinant Friedreich's ataxia familyG Lucotte, S Berriche, J C Turpin
Pageof 20