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P Benlian

Showing results (31-40 of 51) with videos related to

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American Journal of Ophthalmology|March 25, 1998
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degenerationE H Souied, P Benlian, P Amouyel, et al.
Journal of Medical Genetics|November 5, 2002
CYS127S (FH-Kairouan) and D245N (FH-Tozeur) mutations in the LDL receptor gene in Tunisian families with familial hypercholesterolaemiaM N Slimane, S Lestavel, V Clavey, et al.
European Journal of Endocrinology|October 1, 1995
Familial acromegaly: a specific clinical entity--further evidence from the genetic study of a three-generation familyP Benlian, S Giraud, N Lahlou, et al.
Journal of Medical Genetics|August 1, 1997
Assessment of French patients with LPL deficiency for French Canadian mutationsL Foubert, J L De Gennes, J P Lagarde, et al.
American Journal of Human Genetics|May 1, 1991
Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11P Benlian, C Boileau, N Loux, et al.
Infection|August 5, 2004
Major hypertriglyceridemia in HIV-infected patients on antiretroviral therapy: a role of the personal and family historyD Bollens, M Guiguet, P Tangre, et al.
Atherosclerosis|January 16, 1998
Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 alleleL O Abdel-Wareth, S N Pimstone, J P Lagarde, et al.
Atherosclerosis|March 21, 2001
Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian familiesM N Slimane, S Lestavel, X Sun, et al.
Human Genetics|September 1, 1995
Recurrent and novel LDL receptor gene mutations causing heterozygous familial hypercholesterolemia in La HabanaE Pereira, R Ferreira, B Hermelin, et al.
Annales De Genetique|January 1, 1990
A LDL receptor gene homozygous mutation: PCR amplification, direct genomic sequencing, associated haplotype, rapid screening for frequencyP Benlian, S Amselem, N Loux, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
American Journal of Ophthalmology|March 25, 1998
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degenerationE H Souied, P Benlian, P Amouyel, et al.
Journal of Medical Genetics|November 5, 2002
CYS127S (FH-Kairouan) and D245N (FH-Tozeur) mutations in the LDL receptor gene in Tunisian families with familial hypercholesterolaemiaM N Slimane, S Lestavel, V Clavey, et al.
European Journal of Endocrinology|October 1, 1995
Familial acromegaly: a specific clinical entity--further evidence from the genetic study of a three-generation familyP Benlian, S Giraud, N Lahlou, et al.
Journal of Medical Genetics|August 1, 1997
Assessment of French patients with LPL deficiency for French Canadian mutationsL Foubert, J L De Gennes, J P Lagarde, et al.
American Journal of Human Genetics|May 1, 1991
Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11P Benlian, C Boileau, N Loux, et al.
Infection|August 5, 2004
Major hypertriglyceridemia in HIV-infected patients on antiretroviral therapy: a role of the personal and family historyD Bollens, M Guiguet, P Tangre, et al.
Atherosclerosis|January 16, 1998
Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 alleleL O Abdel-Wareth, S N Pimstone, J P Lagarde, et al.
Atherosclerosis|March 21, 2001
Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian familiesM N Slimane, S Lestavel, X Sun, et al.
Human Genetics|September 1, 1995
Recurrent and novel LDL receptor gene mutations causing heterozygous familial hypercholesterolemia in La HabanaE Pereira, R Ferreira, B Hermelin, et al.
Annales De Genetique|January 1, 1990
A LDL receptor gene homozygous mutation: PCR amplification, direct genomic sequencing, associated haplotype, rapid screening for frequencyP Benlian, S Amselem, N Loux, et al.
Pageof 6