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S Berriche

Showing results (11-20 of 24) with videos related to

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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 heterozygotesR Ducrocq, S Berriche, M T Dalle, et al.
Clinical Chemistry|February 1, 1985
Evidence for nonenzymic glycation of antithrombin III in diabetic patientsR 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 FranceG Lucotte, S Berriche, F David, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Trinucleotide GAA repeat expansions in seven French Friedreich ataxia familiesG 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 familyG Lucotte, S Berriche, F David, 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.
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 typesG 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.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 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 heterozygotesR Ducrocq, S Berriche, M T Dalle, et al.
Clinical Chemistry|February 1, 1985
Evidence for nonenzymic glycation of antithrombin III in diabetic patientsR 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 FranceG Lucotte, S Berriche, F David, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Trinucleotide GAA repeat expansions in seven French Friedreich ataxia familiesG 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 familyG Lucotte, S Berriche, F David, 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.
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 typesG 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.
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