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Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Prenatal diagnosis of hereditary amyloidosis in a Portuguese family living in France
G Lucotte, S Berriche, F David, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
Trinucleotide GAA repeat expansions in seven French Friedreich ataxia families
G Lucotte, S Berriche, F David, et al.
Molecular & General Genetics : MGG
|
January 1, 1984
Structural variants of the alpha-fetoprotein gene in different inbred strains of rat
A Gal, J L Nahon, G Lucotte, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Trinucleotide repeat elongation in the huntingtin gene in Huntington's disease patients from 85 French families. The French HD Research Group
G Lucotte, A Aouizérate, O Loreille, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 30, 2009
Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients
G Lucotte, A Houzet, C Hubans, et al.
Molecular and Cellular Probes
|
October 1, 1993
A multiple primer pairs polymerase chain reaction for the detection of human genital papillomavirus types
G Lucotte, M H François, M C Petit, et al.
Human Biology
|
June 1, 1994
Reduced variability in Y-chromosome-specific haplotypes for some Central African populations
G Lucotte, N Gérard, R Krishnamoorthy, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1984
Polymorphism of HLA class I genes after restriction by endonucleases Eco RI, Eco RV and Hind III
G Lucotte, C Coulondre, K Y Ngo, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1987
Taq I polymorphism of HLA class I genes in an ankylosing spondylitis family
G Lucotte, F Huetz, M Mariotti, et al.
Revue Neurologique
|
January 1, 1991
[Presymptomatic diagnosis in Huntington chorea families using the gene amplification technique]
G Lucotte, S Berriche, M C Petit, et al.
Page
of 20
Search research articles
Search
Showing results (161-170 of 199) with videos related to
Sort By:
Page
of 20
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Prenatal diagnosis of hereditary amyloidosis in a Portuguese family living in France
G Lucotte, S Berriche, F David, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
Trinucleotide GAA repeat expansions in seven French Friedreich ataxia families
G Lucotte, S Berriche, F David, et al.
Molecular & General Genetics : MGG
|
January 1, 1984
Structural variants of the alpha-fetoprotein gene in different inbred strains of rat
A Gal, J L Nahon, G Lucotte, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Trinucleotide repeat elongation in the huntingtin gene in Huntington's disease patients from 85 French families. The French HD Research Group
G Lucotte, A Aouizérate, O Loreille, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 30, 2009
Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients
G Lucotte, A Houzet, C Hubans, et al.
Molecular and Cellular Probes
|
October 1, 1993
A multiple primer pairs polymerase chain reaction for the detection of human genital papillomavirus types
G Lucotte, M H François, M C Petit, et al.
Human Biology
|
June 1, 1994
Reduced variability in Y-chromosome-specific haplotypes for some Central African populations
G Lucotte, N Gérard, R Krishnamoorthy, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1984
Polymorphism of HLA class I genes after restriction by endonucleases Eco RI, Eco RV and Hind III
G Lucotte, C Coulondre, K Y Ngo, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1987
Taq I polymorphism of HLA class I genes in an ankylosing spondylitis family
G Lucotte, F Huetz, M Mariotti, et al.
Revue Neurologique
|
January 1, 1991
[Presymptomatic diagnosis in Huntington chorea families using the gene amplification technique]
G Lucotte, S Berriche, M C Petit, et al.
Page
of 20