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N Ghanem

Showing results (41-50 of 144) with videos related to

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European Radiology|May 26, 2006
Detection and characterization of benign focal liver lesions with multislice CTJ T Winterer, E Kotter, N Ghanem, et al.
Annales De Genetique|January 1, 1990
CYP21B gene conversion and complete CYP21A gene deletion in congenital adrenal hyperplasiaJ M Lobaccaro, N Ghanem, G Lefranc, et al.
British Medical Journal (Clinical Research Ed.)|March 28, 1987
Dangers in treating hyponatraemiaA N Ghanem, J A Wojtulewski, M D Penny
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1990
[Molecular genetics of 21-hydroxylase deficiency in congenital adrenal hyperplasia]J M Lobaccaro, N Ghanem, G Lefranc, et al.
Nucleic Acids Research|February 11, 1989
A TaqI RFLP of the human T-cell receptor gamma (TCRG) variable gene V11N Ghanem, P Dariavach, G Lefranc, et al.
Nucleic Acids Research|December 23, 1988
A new TaqI polymorphism of the complement factor B geneJ M Lobaccaro, N Ghanem, C Sultan, et al.
Nucleic Acids Research|May 11, 1989
Identification of the PvuII RFLPs from the switch human immunoglobulin alpha (IGSA) regionsG Keyeux, N Ghanem, G Lefranc, et al.
Nucleic Acids Research|January 11, 1989
A unique RFLP in the human T-cell receptor gamma constant region gene TRGC1N Ghanem, C Buresi, G Lefranc, et al.
Molecular and Cellular Probes|April 1, 1993
Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemiasN Ghanem, M Vidaud, F Plassa, et al.
Experimental and Clinical Immunogenetics|January 1, 1989
BstEII restriction fragment alleles and haplotypes of the human IGHG genes with reference to the BamHI/SacI RFLPs and to the Gm polymorphismN Ghanem, J M Dugoujon, M P Lefranc, et al.
Pageof 15

Showing results (41-50 of 144) with videos related to

Sort By:
Pageof 15
European Radiology|May 26, 2006
Detection and characterization of benign focal liver lesions with multislice CTJ T Winterer, E Kotter, N Ghanem, et al.
Annales De Genetique|January 1, 1990
CYP21B gene conversion and complete CYP21A gene deletion in congenital adrenal hyperplasiaJ M Lobaccaro, N Ghanem, G Lefranc, et al.
British Medical Journal (Clinical Research Ed.)|March 28, 1987
Dangers in treating hyponatraemiaA N Ghanem, J A Wojtulewski, M D Penny
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1990
[Molecular genetics of 21-hydroxylase deficiency in congenital adrenal hyperplasia]J M Lobaccaro, N Ghanem, G Lefranc, et al.
Nucleic Acids Research|February 11, 1989
A TaqI RFLP of the human T-cell receptor gamma (TCRG) variable gene V11N Ghanem, P Dariavach, G Lefranc, et al.
Nucleic Acids Research|December 23, 1988
A new TaqI polymorphism of the complement factor B geneJ M Lobaccaro, N Ghanem, C Sultan, et al.
Nucleic Acids Research|May 11, 1989
Identification of the PvuII RFLPs from the switch human immunoglobulin alpha (IGSA) regionsG Keyeux, N Ghanem, G Lefranc, et al.
Nucleic Acids Research|January 11, 1989
A unique RFLP in the human T-cell receptor gamma constant region gene TRGC1N Ghanem, C Buresi, G Lefranc, et al.
Molecular and Cellular Probes|April 1, 1993
Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemiasN Ghanem, M Vidaud, F Plassa, et al.
Experimental and Clinical Immunogenetics|January 1, 1989
BstEII restriction fragment alleles and haplotypes of the human IGHG genes with reference to the BamHI/SacI RFLPs and to the Gm polymorphismN Ghanem, J M Dugoujon, M P Lefranc, et al.
Pageof 15