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European Radiology
|
May 26, 2006
Detection and characterization of benign focal liver lesions with multislice CT
J 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 hyperplasia
J M Lobaccaro, N Ghanem, G Lefranc, et al.
British Medical Journal (Clinical Research Ed.)
|
March 28, 1987
Dangers in treating hyponatraemia
A 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 V11
N Ghanem, P Dariavach, G Lefranc, et al.
Nucleic Acids Research
|
December 23, 1988
A new TaqI polymorphism of the complement factor B gene
J 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) regions
G 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 TRGC1
N 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-thalassemias
N 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 polymorphism
N Ghanem, J M Dugoujon, M P Lefranc, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 144) with videos related to
Sort By:
Page
of 15
European Radiology
|
May 26, 2006
Detection and characterization of benign focal liver lesions with multislice CT
J 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 hyperplasia
J M Lobaccaro, N Ghanem, G Lefranc, et al.
British Medical Journal (Clinical Research Ed.)
|
March 28, 1987
Dangers in treating hyponatraemia
A 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 V11
N Ghanem, P Dariavach, G Lefranc, et al.
Nucleic Acids Research
|
December 23, 1988
A new TaqI polymorphism of the complement factor B gene
J 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) regions
G 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 TRGC1
N 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-thalassemias
N 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 polymorphism
N Ghanem, J M Dugoujon, M P Lefranc, et al.
Page
of 15