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J C Turpin

Showing results (51-60 of 88) with videos related to

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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.
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.
Annales De Radiologie|January 1, 1970
[Subclavian arteriography in the study of malformations of the supraclavicular fossa]J Bories, J Rosier, D Fredy, 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
Trinucleotide repeat elongation in the huntingtin gene in Huntington's disease patients from 85 French families. The French HD Research GroupG Lucotte, A Aouizérate, O Loreille, et al.
Psychiatry Research|October 1, 1989
Arylsulfatase A activity among psychotic patientsM Lejoyeux, G Dubois, J C Turpin, et al.
Archives Francaises De Pediatrie|March 1, 1982
[Iconographic rubric. Diplomyelia]E Questiaux, Z Joannides, O Bacques, et al.
La Nouvelle Presse Medicale|April 26, 1980
[Value of the estimation of gliofibrillary acid protein in the diagnosis of glial tumours (author's transl)]J C Turpin, C Jacque, M Pluot, et al.
Revue Neurologique|January 1, 1985
[Adult disclosure of a case of familial adrenoleukodystrophy]J C Turpin, M Paturneau-Jouas, C Sereni, 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.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
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.
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.
Annales De Radiologie|January 1, 1970
[Subclavian arteriography in the study of malformations of the supraclavicular fossa]J Bories, J Rosier, D Fredy, 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
Trinucleotide repeat elongation in the huntingtin gene in Huntington's disease patients from 85 French families. The French HD Research GroupG Lucotte, A Aouizérate, O Loreille, et al.
Psychiatry Research|October 1, 1989
Arylsulfatase A activity among psychotic patientsM Lejoyeux, G Dubois, J C Turpin, et al.
Archives Francaises De Pediatrie|March 1, 1982
[Iconographic rubric. Diplomyelia]E Questiaux, Z Joannides, O Bacques, et al.
La Nouvelle Presse Medicale|April 26, 1980
[Value of the estimation of gliofibrillary acid protein in the diagnosis of glial tumours (author's transl)]J C Turpin, C Jacque, M Pluot, et al.
Revue Neurologique|January 1, 1985
[Adult disclosure of a case of familial adrenoleukodystrophy]J C Turpin, M Paturneau-Jouas, C Sereni, 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.
Pageof 9