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Annales De Dermatologie Et De Venereologie
|
October 11, 2007
[NF1: Molecular testing in clinical practice]
C Rieubland, D Vidaud, S Jacquemont
Archives Francaises De Pediatrie
|
May 1, 1988
[Hereditary persistence of fetal hemoglobin associated with mutation above the gamma gene]
D Vidaud-Raphanaud, J Badoual, D Labie
Annales De Genetique
|
January 1, 1988
Interaction of deletional alpha-thalassaemia with sickle cell beta-thalassaemia and its influence on foetal haemoglobin expression
D Vidaud-Raphanaud, R Krishnamoorthy, G Schaison, et al.
Annales De Genetique
|
January 1, 1987
[Analysis of the recombination zone in hereditary persistence of fetal hemoglobin with fetal gene rearrangement of the G gamma-G gamma-A gamma type]
D Vidaud-Raphanaud, E Bouhassira, D Labie, 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.
Molecular and Biochemical Parasitology
|
June 1, 1991
Structure of the Echinococcus multilocularis U1 snRNA gene repeat
S Bretagne, B Robert, D Vidaud, et al.
Thyroid : Official Journal of the American Thyroid Association
|
April 6, 2001
Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reaction
I Bièche, B Franc, D Vidaud, et al.
Experimental Parasitology
|
April 1, 1996
Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genes
S Bretagne, B Assouline, D Vidaud, et al.
Neurology
|
May 1, 1996
Misdiagnosis revealed by genetic linkage analysis in a family with Wilson disease
D Vidaud, B Assouline, P Lecoz, et al.
Annales De Dermatologie Et De Venereologie
|
February 22, 2011
[McCune-Albright syndrome]
A Saussine, L Valeyrie-Allanore, D Vidaud, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 70) with videos related to
Sort By:
Page
of 7
Annales De Dermatologie Et De Venereologie
|
October 11, 2007
[NF1: Molecular testing in clinical practice]
C Rieubland, D Vidaud, S Jacquemont
Archives Francaises De Pediatrie
|
May 1, 1988
[Hereditary persistence of fetal hemoglobin associated with mutation above the gamma gene]
D Vidaud-Raphanaud, J Badoual, D Labie
Annales De Genetique
|
January 1, 1988
Interaction of deletional alpha-thalassaemia with sickle cell beta-thalassaemia and its influence on foetal haemoglobin expression
D Vidaud-Raphanaud, R Krishnamoorthy, G Schaison, et al.
Annales De Genetique
|
January 1, 1987
[Analysis of the recombination zone in hereditary persistence of fetal hemoglobin with fetal gene rearrangement of the G gamma-G gamma-A gamma type]
D Vidaud-Raphanaud, E Bouhassira, D Labie, 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.
Molecular and Biochemical Parasitology
|
June 1, 1991
Structure of the Echinococcus multilocularis U1 snRNA gene repeat
S Bretagne, B Robert, D Vidaud, et al.
Thyroid : Official Journal of the American Thyroid Association
|
April 6, 2001
Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reaction
I Bièche, B Franc, D Vidaud, et al.
Experimental Parasitology
|
April 1, 1996
Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genes
S Bretagne, B Assouline, D Vidaud, et al.
Neurology
|
May 1, 1996
Misdiagnosis revealed by genetic linkage analysis in a family with Wilson disease
D Vidaud, B Assouline, P Lecoz, et al.
Annales De Dermatologie Et De Venereologie
|
February 22, 2011
[McCune-Albright syndrome]
A Saussine, L Valeyrie-Allanore, D Vidaud, et al.
Page
of 7