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Revue Neurologique
|
January 1, 1990
[Use of polymorphous DNA probes in the study of French families with Huntington's chorea]
G Lucotte, S Berriche, A Burckel, et al.
Clinical Chemistry
|
August 1, 1984
Rapid quantification of Hb Hope in heterozygotes
R Ducrocq, S Berriche, M T Dalle, et al.
Clinical Chemistry
|
February 1, 1985
Evidence for nonenzymic glycation of antithrombin III in diabetic patients
R Ducrocq, H Bachour, R Belkhodja, et al.
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.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family
G Lucotte, S Berriche, F David, et al.
Annales De Genetique
|
January 1, 1992
Manic depressive illness is linked to factor IX in a French pedigree
G Lucotte, A Landoulsi, S Berriche, 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.
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.
Presse Medicale (Paris, France : 1983)
|
December 19, 1992
[Prenatal diagnosis in a family affected by amyloid neuropathy]
J C Turpin, S Berriche, F David, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Revue Neurologique
|
January 1, 1990
[Use of polymorphous DNA probes in the study of French families with Huntington's chorea]
G Lucotte, S Berriche, A Burckel, et al.
Clinical Chemistry
|
August 1, 1984
Rapid quantification of Hb Hope in heterozygotes
R Ducrocq, S Berriche, M T Dalle, et al.
Clinical Chemistry
|
February 1, 1985
Evidence for nonenzymic glycation of antithrombin III in diabetic patients
R Ducrocq, H Bachour, R Belkhodja, et al.
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.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family
G Lucotte, S Berriche, F David, et al.
Annales De Genetique
|
January 1, 1992
Manic depressive illness is linked to factor IX in a French pedigree
G Lucotte, A Landoulsi, S Berriche, 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.
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.
Presse Medicale (Paris, France : 1983)
|
December 19, 1992
[Prenatal diagnosis in a family affected by amyloid neuropathy]
J C Turpin, S Berriche, F David, et al.
Page
of 3