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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 dystrophy
K 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 old
G 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 tumor
L 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 neuroblastoma
G 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 gliomas
P 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 heterogeneity
L 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 mutations
D A Pillers, K M Fitzgerald, N M Duncan, et al.
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Search research articles
Search
Showing results (71-80 of 86) with videos related to
Sort By:
Page
of 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 dystrophy
K 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 old
G 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 tumor
L 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 neuroblastoma
G 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 gliomas
P 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 heterogeneity
L 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 mutations
D A Pillers, K M Fitzgerald, N M Duncan, et al.
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of 9