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F Hentati

Showing results (91-100 of 120) with videos related to

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Neurology|December 1, 1990
Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophyS Ben Jelloun-Dellagi, P Chaffey, F Hentati, et al.
Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
European Journal of Neurology|October 10, 2012
Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disordersM B Hammer, G Eleuch-Fayache, J R Gibbs, et al.
Nature Genetics|July 1, 1994
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35A Hentati, K Bejaoui, M A Pericak-Vance, et al.
Parkinsonism & Related Disorders|April 17, 2007
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's diseaseL Warren, R Gibson, L Ishihara, et al.
Nature Genetics|November 4, 2000
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathyP Bomont, L Cavalier, F Blondeau, et al.
Neurology|April 23, 2003
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2IA Driss, S Noguchi, R Amouri, et al.
Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
Genomics|May 8, 1998
Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13J Liu, C Wu, K Bossie, et al.
Genomics|January 25, 2000
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15K B Othmane, E Johnson, M Menold, et al.
Pageof 12

Showing results (91-100 of 120) with videos related to

Sort By:
Pageof 12
Neurology|December 1, 1990
Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophyS Ben Jelloun-Dellagi, P Chaffey, F Hentati, et al.
Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
European Journal of Neurology|October 10, 2012
Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disordersM B Hammer, G Eleuch-Fayache, J R Gibbs, et al.
Nature Genetics|July 1, 1994
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35A Hentati, K Bejaoui, M A Pericak-Vance, et al.
Parkinsonism & Related Disorders|April 17, 2007
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's diseaseL Warren, R Gibson, L Ishihara, et al.
Nature Genetics|November 4, 2000
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathyP Bomont, L Cavalier, F Blondeau, et al.
Neurology|April 23, 2003
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2IA Driss, S Noguchi, R Amouri, et al.
Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
Genomics|May 8, 1998
Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13J Liu, C Wu, K Bossie, et al.
Genomics|January 25, 2000
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15K B Othmane, E Johnson, M Menold, et al.
Pageof 12