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La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|February 8, 1981
[Interest of ganglioside analysis in the neuroblastoma (author's transl)]N Baumann, J C Turpin, R Gérard-Marchand, 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.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
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.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.Developmental Neuroscience|January 1, 1991
Adult forms of metachromatic leukodystrophy: clinical and biochemical approachN Baumann, M Masson, V Carreau, et al.Pageof 7