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Nucleic Acids Research
|
February 11, 1989
A new TaqI allele at DXS52 frequent in Algeria
K 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-DeltaE126
P 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 France
G 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 chromatography
A 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 diagnosis
L 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 synthesis
C Bonne-Andrea, F Harper, E Puvion, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 96) with videos related to
Sort By:
Page
of 10
Nucleic Acids Research
|
February 11, 1989
A new TaqI allele at DXS52 frequent in Algeria
K 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-DeltaE126
P 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 France
G 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 chromatography
A 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 diagnosis
L 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 synthesis
C Bonne-Andrea, F Harper, E Puvion, et al.
Page
of 10