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La Revue Du Praticien
|
January 15, 1997
[Mechanisms and consequences of genetic mutations]
M Vidaud
La Revue Du Praticien
|
December 21, 1989
[Prenatal diagnosis of hemophilia A and B]
M Vidaud, J M Lavergne
Archives Francaises De Pediatrie
|
October 1, 1985
[Association of hemoglobin E and thalassemia]
G Schaison, G Leverger, M Vidaud
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1986
[Alpha-thalassemia in Tunisia: molecular bases of hemoglobinosis H]
S Abbes, M Vidaud, S Fattoum, et al.
Hepatology (Baltimore, Md.)
|
October 2, 1998
Clonal analysis of macronodules in cirrhosis
V Paradis, I Laurendeau, M Vidaud, et al.
Pathologie-Biologie
|
January 1, 1988
[Detection of residual disease in onco-hematology: the contribution of molecular biology]
T Henni, M Vidaud, S Bretagne, et al.
Hemoglobin
|
January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expression
S Abbes, S Fattoum, M Vidaud, et al.
Molecular and Cellular Probes
|
April 1, 1993
Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemias
N Ghanem, M Vidaud, F Plassa, et al.
Human Mutation
|
December 19, 2001
Identification and characterization of four novel large deletions in the human neurofibromatosis type 1 (NF1) gene
L J Fang, D Vidaud, M Vidaud, et al.
Carcinogenesis
|
September 5, 2001
Quantitation of androgen receptor gene expression in sporadic breast tumors by real-time RT-PCR: evidence that MYC is an AR-regulated gene
I Bièche, B Parfait, S Tozlu, et al.
Page
of 14
Search research articles
Search
Showing results (1-10 of 135) with videos related to
Sort By:
Page
of 14
La Revue Du Praticien
|
January 15, 1997
[Mechanisms and consequences of genetic mutations]
M Vidaud
La Revue Du Praticien
|
December 21, 1989
[Prenatal diagnosis of hemophilia A and B]
M Vidaud, J M Lavergne
Archives Francaises De Pediatrie
|
October 1, 1985
[Association of hemoglobin E and thalassemia]
G Schaison, G Leverger, M Vidaud
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1986
[Alpha-thalassemia in Tunisia: molecular bases of hemoglobinosis H]
S Abbes, M Vidaud, S Fattoum, et al.
Hepatology (Baltimore, Md.)
|
October 2, 1998
Clonal analysis of macronodules in cirrhosis
V Paradis, I Laurendeau, M Vidaud, et al.
Pathologie-Biologie
|
January 1, 1988
[Detection of residual disease in onco-hematology: the contribution of molecular biology]
T Henni, M Vidaud, S Bretagne, et al.
Hemoglobin
|
January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expression
S Abbes, S Fattoum, M Vidaud, et al.
Molecular and Cellular Probes
|
April 1, 1993
Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemias
N Ghanem, M Vidaud, F Plassa, et al.
Human Mutation
|
December 19, 2001
Identification and characterization of four novel large deletions in the human neurofibromatosis type 1 (NF1) gene
L J Fang, D Vidaud, M Vidaud, et al.
Carcinogenesis
|
September 5, 2001
Quantitation of androgen receptor gene expression in sporadic breast tumors by real-time RT-PCR: evidence that MYC is an AR-regulated gene
I Bièche, B Parfait, S Tozlu, et al.
Page
of 14