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G Lucotte

Showing results (151-160 of 199) with videos related to

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Biochemical Genetics|December 1, 1982
Eco RI restriction-site polymorphism of the albumin gene in different inbred strains of ratG Lucotte, A Gal, J L Nahon, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French familyG Lucotte, S Berriche, F David, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) familyK Fontaine, O Sémonin, J P Legarde, et al.
American Journal of Human Genetics|April 1, 1986
A DNA probe detecting multiple haplotypes of the human Y chromosomeK Y Ngo, G Vergnaud, C Johnsson, et al.
Annales De Genetique|January 1, 1992
Manic depressive illness is linked to factor IX in a French pedigreeG Lucotte, A Landoulsi, S Berriche, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Genetic counseling in a French Friedreich's ataxia familyG Lucotte, G Mercier, B Sablonière, et al.
European Journal of Neurology|April 6, 2004
Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's diseaseO Santt, H Baranova, E Albuisson, et al.
Molecular and Cellular Probes|December 1, 1994
Detection of serum hepatitis B virus using a nested polymerase chain reaction assayG Lucotte, P Galzot, C Y Lu, et al.
American Journal of Medical Genetics|July 26, 1996
Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in familiesG Lucotte, J C Turpin, N Gérard, et al.
American Journal of Medical Genetics|December 18, 1995
Allele doses of apolipoprotein E type epsilon 4 in sporadic late-onset Alzheimer's diseaseG Lucotte, A Aouizérate, N Gérard, et al.
Pageof 20

Showing results (151-160 of 199) with videos related to

Sort By:
Pageof 20
Biochemical Genetics|December 1, 1982
Eco RI restriction-site polymorphism of the albumin gene in different inbred strains of ratG Lucotte, A Gal, J L Nahon, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French familyG Lucotte, S Berriche, F David, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) familyK Fontaine, O Sémonin, J P Legarde, et al.
American Journal of Human Genetics|April 1, 1986
A DNA probe detecting multiple haplotypes of the human Y chromosomeK Y Ngo, G Vergnaud, C Johnsson, et al.
Annales De Genetique|January 1, 1992
Manic depressive illness is linked to factor IX in a French pedigreeG Lucotte, A Landoulsi, S Berriche, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Genetic counseling in a French Friedreich's ataxia familyG Lucotte, G Mercier, B Sablonière, et al.
European Journal of Neurology|April 6, 2004
Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's diseaseO Santt, H Baranova, E Albuisson, et al.
Molecular and Cellular Probes|December 1, 1994
Detection of serum hepatitis B virus using a nested polymerase chain reaction assayG Lucotte, P Galzot, C Y Lu, et al.
American Journal of Medical Genetics|July 26, 1996
Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in familiesG Lucotte, J C Turpin, N Gérard, et al.
American Journal of Medical Genetics|December 18, 1995
Allele doses of apolipoprotein E type epsilon 4 in sporadic late-onset Alzheimer's diseaseG Lucotte, A Aouizérate, N Gérard, et al.
Pageof 20