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M Delpech

Showing results (41-50 of 96) with videos related to

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Nucleic Acids Research|February 11, 1989
A new TaqI allele at DXS52 frequent in AlgeriaK Nafa, A Reghis, M Benabadji, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 24, 2000
A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI gene-R124L and DeltaT125-DeltaE126P Dighiero, S Drunat, F D'Hermies, et al.
Clinical Genetics|March 1, 1993
Late-onset familial amyloid polyneuropathy with the TTR Met 30 mutation in FranceG Grateau, D Adams, D Malapert, et al.
Journal of Chromatography|November 8, 1985
Analysis and preparation of chromosomal high-mobility group proteins by ion-exchange high-performance liquid chromatographyA Riffe, M Delpech, F Levy-Favatier, et al.
American Journal of Medical Genetics|January 8, 1999
Potential pitfall in Prader-Willi syndrome and Angelman syndrome molecular diagnosisL Cuisset, C Vasseur, M Jeanpierre, et al.
La Revue De Medecine Interne|July 26, 2000
[Diagnostic strategy in amyloidosis]G Grateau, H Lebrazi, S Valleix, et al.
La Revue De Medecine Interne|December 6, 2003
[Tumor necrosis factor receptor superfamily 1A-associated periodic syndrome (TRAPS)]V Hentgen, B Granel, C Dodé, et al.
Annales De Genetique|February 16, 2000
[French Society for Human Genetics. "Genetics in Practice" Commission. Core scientific data of use in genetic counseling. Familial Mediterranean fever]C Cazeneuve, C Dode, M Delpech, et al.
Annales De Biologie Clinique|January 1, 1995
[Evaluation of assay methods of glycohemoglobin: reference method and parameter]P Gillery, M Delpech, I Garcia, et al.
Biology of the Cell|January 1, 1986
Nuclear accumulation of HMG1 protein is correlated to DNA synthesisC Bonne-Andrea, F Harper, E Puvion, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Nucleic Acids Research|February 11, 1989
A new TaqI allele at DXS52 frequent in AlgeriaK Nafa, A Reghis, M Benabadji, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 24, 2000
A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI gene-R124L and DeltaT125-DeltaE126P Dighiero, S Drunat, F D'Hermies, et al.
Clinical Genetics|March 1, 1993
Late-onset familial amyloid polyneuropathy with the TTR Met 30 mutation in FranceG Grateau, D Adams, D Malapert, et al.
Journal of Chromatography|November 8, 1985
Analysis and preparation of chromosomal high-mobility group proteins by ion-exchange high-performance liquid chromatographyA Riffe, M Delpech, F Levy-Favatier, et al.
American Journal of Medical Genetics|January 8, 1999
Potential pitfall in Prader-Willi syndrome and Angelman syndrome molecular diagnosisL Cuisset, C Vasseur, M Jeanpierre, et al.
La Revue De Medecine Interne|July 26, 2000
[Diagnostic strategy in amyloidosis]G Grateau, H Lebrazi, S Valleix, et al.
La Revue De Medecine Interne|December 6, 2003
[Tumor necrosis factor receptor superfamily 1A-associated periodic syndrome (TRAPS)]V Hentgen, B Granel, C Dodé, et al.
Annales De Genetique|February 16, 2000
[French Society for Human Genetics. "Genetics in Practice" Commission. Core scientific data of use in genetic counseling. Familial Mediterranean fever]C Cazeneuve, C Dode, M Delpech, et al.
Annales De Biologie Clinique|January 1, 1995
[Evaluation of assay methods of glycohemoglobin: reference method and parameter]P Gillery, M Delpech, I Garcia, et al.
Biology of the Cell|January 1, 1986
Nuclear accumulation of HMG1 protein is correlated to DNA synthesisC Bonne-Andrea, F Harper, E Puvion, et al.
Pageof 10