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A Benomar

Showing results (61-70 of 77) with videos related to

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Annales De Biologie Clinique|June 26, 2004
[Apolipoprotein E and angiotensin-converting enzyme gene polymorphisms as risk factors of coronary disease]N Bennouar, A Allami, A Laraqui, et al.
Journal of Medical Genetics|June 3, 1999
Linkage disequilibrium at the SCA2 locusO Didierjean, G Cancel, G Stevanin, et al.
Annales De Cardiologie Et D'Angeiologie|June 19, 2007
[Takayasu's arteritis revealed by aortic regurgitation with ascending aortic aneurysm (About 2 cases)]M El Kouache, L Marmade, M Tribak, et al.
Annales De Biologie Clinique|October 9, 2002
[Homocysteine, lipoprotein (a): risk factors for coronary heart disease]A Laraqui, N Bennouar, F Meggouh, et al.
American Journal of Human Genetics|August 12, 1999
A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3A Bouhouche, A Benomar, N Birouk, et al.
Animal Genetics|April 29, 2009
PRNP haplotype distribution in Moroccan goatsC Serrano, M Hammouchi, A Benomar, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Revue Neurologique|March 12, 2018
Association of vitamin D status with multiple sclerosis in a case-control study from MoroccoA Skalli, E H Ait Ben Haddou, R El Jaoudi, et al.
Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
Annales De Biologie Clinique|June 26, 2004
[Apolipoprotein E and angiotensin-converting enzyme gene polymorphisms as risk factors of coronary disease]N Bennouar, A Allami, A Laraqui, et al.
Journal of Medical Genetics|June 3, 1999
Linkage disequilibrium at the SCA2 locusO Didierjean, G Cancel, G Stevanin, et al.
Annales De Cardiologie Et D'Angeiologie|June 19, 2007
[Takayasu's arteritis revealed by aortic regurgitation with ascending aortic aneurysm (About 2 cases)]M El Kouache, L Marmade, M Tribak, et al.
Annales De Biologie Clinique|October 9, 2002
[Homocysteine, lipoprotein (a): risk factors for coronary heart disease]A Laraqui, N Bennouar, F Meggouh, et al.
American Journal of Human Genetics|August 12, 1999
A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3A Bouhouche, A Benomar, N Birouk, et al.
Animal Genetics|April 29, 2009
PRNP haplotype distribution in Moroccan goatsC Serrano, M Hammouchi, A Benomar, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Revue Neurologique|March 12, 2018
Association of vitamin D status with multiple sclerosis in a case-control study from MoroccoA Skalli, E H Ait Ben Haddou, R El Jaoudi, et al.
Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
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