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G W Padberg

Showing results (51-60 of 114) with videos related to

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Muscle & Nerve. Supplement|January 1, 1995
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.
American Journal of Human Genetics|August 12, 1999
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch familyH T Verzijl, B van den Helm, B Veldman, et al.
Muscle & Nerve. Supplement|April 12, 2013
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.
Journal of Neurology|February 25, 2005
Cognitive evaluation in adult patients with Möbius syndromeH T F M Verzijl, N van Es, H J C Berger, et al.
Human Genetics|April 1, 1994
Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genomeJ C van Deutekom, R P Bruyn, N van den Boorn, et al.
Magnetic Resonance in Medicine|October 13, 2006
Intake of 13C-4 creatine enables simultaneous assessment of creatine and phosphocreatine pools in human skeletal muscle by 13C MR spectroscopyH E Kan, M van der Graaf, D W J Klomp, et al.
Muscle & Nerve. Supplement|April 12, 2013
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Muscle & Nerve. Supplement|January 1, 1995
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Genomics|January 1, 1994
Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletionsC Wijmenga, J C van Deutekom, J E Hewitt, et al.
Pageof 12

Showing results (51-60 of 114) with videos related to

Sort By:
Pageof 12
Muscle & Nerve. Supplement|January 1, 1995
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.
American Journal of Human Genetics|August 12, 1999
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch familyH T Verzijl, B van den Helm, B Veldman, et al.
Muscle & Nerve. Supplement|April 12, 2013
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.
Journal of Neurology|February 25, 2005
Cognitive evaluation in adult patients with Möbius syndromeH T F M Verzijl, N van Es, H J C Berger, et al.
Human Genetics|April 1, 1994
Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genomeJ C van Deutekom, R P Bruyn, N van den Boorn, et al.
Magnetic Resonance in Medicine|October 13, 2006
Intake of 13C-4 creatine enables simultaneous assessment of creatine and phosphocreatine pools in human skeletal muscle by 13C MR spectroscopyH E Kan, M van der Graaf, D W J Klomp, et al.
Muscle & Nerve. Supplement|April 12, 2013
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Muscle & Nerve. Supplement|January 1, 1995
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Genomics|January 1, 1994
Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletionsC Wijmenga, J C van Deutekom, J E Hewitt, et al.
Pageof 12