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Molecular and Cellular Probes
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December 1, 1996
A simplified semiquantitative determination of hepatitis C virus genome molecules by the end-point dilution method
C Bathelier, G Mercier, G Lucotte
Lancet (London, England)
|
October 5, 1991
North-west/south-east gradient in delta F508 frequency in Europe
G Lucotte, S Hazout, F Loirat
Human Genetics
|
October 1, 1991
Frequency of the cystic fibrosis mutation delta F508 in Algeria
G Lucotte, E Barré, S Berriche
Blood Cells, Molecules & Diseases
|
January 11, 2002
A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D
G Lucotte, T Champenois, O Sémonin
Human Immunology
|
September 7, 2001
North African genes in Iberia studied by Y-chromosome DNA haplotype V
G Lucotte, N Gérard, G Mercier
Genetic Counseling (Geneva, Switzerland)
|
August 9, 2001
Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1 in a French family
G Lucotte, O Sémonin, G Mercier
Experimental and Clinical Immunogenetics
|
January 1, 1987
Taq I restriction polymorphism of HLA class-I genes, and hybridization with HLA-A and HLA-B specific probes
F Huetz, M Mariotti, G Lucotte
Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
Screening for the M694V mutation of the familial Mediterranean fever (FMF) gene in 604 French patients
C Bathelier, G Lenoir, G Lucotte
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1987
[Absence of linkage between Alzheimer's disease and a polymorphic probe of the long arm of chromosome 21]
F David, L Hallé, G Lucotte
Annales De Genetique
|
January 1, 1992
[Familial Alzheimer's disease in France: results of a preliminary survey]
G Lucotte, F David, S Hazout
Page
of 20
Search research articles
Search
Showing results (91-100 of 199) with videos related to
Sort By:
Page
of 20
Molecular and Cellular Probes
|
December 1, 1996
A simplified semiquantitative determination of hepatitis C virus genome molecules by the end-point dilution method
C Bathelier, G Mercier, G Lucotte
Lancet (London, England)
|
October 5, 1991
North-west/south-east gradient in delta F508 frequency in Europe
G Lucotte, S Hazout, F Loirat
Human Genetics
|
October 1, 1991
Frequency of the cystic fibrosis mutation delta F508 in Algeria
G Lucotte, E Barré, S Berriche
Blood Cells, Molecules & Diseases
|
January 11, 2002
A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D
G Lucotte, T Champenois, O Sémonin
Human Immunology
|
September 7, 2001
North African genes in Iberia studied by Y-chromosome DNA haplotype V
G Lucotte, N Gérard, G Mercier
Genetic Counseling (Geneva, Switzerland)
|
August 9, 2001
Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1 in a French family
G Lucotte, O Sémonin, G Mercier
Experimental and Clinical Immunogenetics
|
January 1, 1987
Taq I restriction polymorphism of HLA class-I genes, and hybridization with HLA-A and HLA-B specific probes
F Huetz, M Mariotti, G Lucotte
Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
Screening for the M694V mutation of the familial Mediterranean fever (FMF) gene in 604 French patients
C Bathelier, G Lenoir, G Lucotte
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1987
[Absence of linkage between Alzheimer's disease and a polymorphic probe of the long arm of chromosome 21]
F David, L Hallé, G Lucotte
Annales De Genetique
|
January 1, 1992
[Familial Alzheimer's disease in France: results of a preliminary survey]
G Lucotte, F David, S Hazout
Page
of 20