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W Cibis

Showing results (71-80 of 86) with videos related to

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Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|June 15, 2016
[Future Trends in Medical Rehabilitation in the Context of Multimorbidity - Part II: Structural Requirements to Manage an Appropriate Rehabilitative Healthcare]W Seger, W Cibis, A Deventer, et al.
Journal of Medical Genetics|May 5, 1999
ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophyK M Fitzgerald, G W Cibis, A H Gettel, et al.
Annals of Ophthalmology|August 1, 1985
The Parsons visual acuity test for screening children 18 to 48 months oldG W Cibis, J H Maino, M A Crandall, et al.
Journal of Pediatric Ophthalmology and Strabismus|May 1, 1993
Aneurysmal bone cyst: report of a case mimicking orbital tumorL A Bealer, G W Cibis, B F Barker, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|June 15, 2016
[Future Trends in Medical Rehabilitation in the Context of Multimorbidity - Part I: Definition of Terms, Issues and Challenges]W Seger, W Cibis, A Deventer, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|July 2, 2016
[Correction: Future Trends in Medical Rehabilitation in the Context of Multimorbidity - Part I: Definition of Terms, Issues and Challenges]W Seger, W Cibis, A Deventer, et al.
American Journal of Ophthalmology|April 15, 1990
Bilateral choroidal neonatal neuroblastomaG W Cibis, A I Freeman, V Pang, et al.
Molecular Carcinogenesis|June 1, 1997
A deletion polymorphism due to Alu-Alu recombination in intron 2 of the retinoblastoma gene: association with human gliomasP G Rothberg, S Ponnuru, D Baker, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 25, 2001
Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneityL A Donoso, A T Frost, E M Stone, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|June 15, 2016
[Future Trends in Medical Rehabilitation in the Context of Multimorbidity - Part II: Structural Requirements to Manage an Appropriate Rehabilitative Healthcare]W Seger, W Cibis, A Deventer, et al.
Journal of Medical Genetics|May 5, 1999
ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophyK M Fitzgerald, G W Cibis, A H Gettel, et al.
Annals of Ophthalmology|August 1, 1985
The Parsons visual acuity test for screening children 18 to 48 months oldG W Cibis, J H Maino, M A Crandall, et al.
Journal of Pediatric Ophthalmology and Strabismus|May 1, 1993
Aneurysmal bone cyst: report of a case mimicking orbital tumorL A Bealer, G W Cibis, B F Barker, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|June 15, 2016
[Future Trends in Medical Rehabilitation in the Context of Multimorbidity - Part I: Definition of Terms, Issues and Challenges]W Seger, W Cibis, A Deventer, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|July 2, 2016
[Correction: Future Trends in Medical Rehabilitation in the Context of Multimorbidity - Part I: Definition of Terms, Issues and Challenges]W Seger, W Cibis, A Deventer, et al.
American Journal of Ophthalmology|April 15, 1990
Bilateral choroidal neonatal neuroblastomaG W Cibis, A I Freeman, V Pang, et al.
Molecular Carcinogenesis|June 1, 1997
A deletion polymorphism due to Alu-Alu recombination in intron 2 of the retinoblastoma gene: association with human gliomasP G Rothberg, S Ponnuru, D Baker, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 25, 2001
Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneityL A Donoso, A T Frost, E M Stone, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Pageof 9