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E Schwinger

Showing results (81-90 of 213) with videos related to

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Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 13, 2001
R124C mutation of the betaIGH3 gene leads to remarkable phenotypic variability in a Greek four-generation family with lattice corneal dystrophy type 1Y Hellenbroich, G Tzivras, B Neppert, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1993
[Molecular genetic diagnosis of Wiskott-Aldrich syndrome]U Orth, W Rosenkranz, E Schwinger, et al.
Human Genetics|January 1, 1995
Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28M Rathmann, S Bunge, C Steglich, et al.
Nature Genetics|May 1, 1994
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindnessA Gal, U Orth, W Baehr, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|May 1, 1990
Dynamic left ventricular outflow obstruction after aortic valve replacement: a Doppler echocardiographic studyM E Schwinger, F O'Brien, R S Freedberg, et al.
European Archives of Psychiatry and Clinical Neuroscience|January 1, 1996
Eye tracking dysfunction in families with multiple cases of schizophreniaV Arolt, R Lencer, A Nolte, et al.
Klinische Monatsblatter Fur Augenheilkunde|June 1, 1992
[Bilateral colobomatous microphthalmus with orbital giant cysts in incomplete tetrasomy 22]W Lange, R Rochels, J Otte, et al.
HNO|August 1, 1996
[Familial occurrence of oculoauricolovertebral dysplasia and Franceschetti syndrome]U Bestelmeyer, H Weerda, R Siegert, et al.
Prenatal Diagnosis|January 13, 1999
Sonographically detected fetal and placental abnormalities associated with trisomy 16 confined to the placenta. A case report and review of the literatureA Astner, E Schwinger, A Caliebe, et al.
Journal of Neurology|July 7, 2005
Spinocerebellar ataxia type 4. Investigation of 34 candidate genesY Hellenbroich, H Pawlack, U Rüb, et al.
Pageof 22

Showing results (81-90 of 213) with videos related to

Sort By:
Pageof 22
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 13, 2001
R124C mutation of the betaIGH3 gene leads to remarkable phenotypic variability in a Greek four-generation family with lattice corneal dystrophy type 1Y Hellenbroich, G Tzivras, B Neppert, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1993
[Molecular genetic diagnosis of Wiskott-Aldrich syndrome]U Orth, W Rosenkranz, E Schwinger, et al.
Human Genetics|January 1, 1995
Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28M Rathmann, S Bunge, C Steglich, et al.
Nature Genetics|May 1, 1994
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindnessA Gal, U Orth, W Baehr, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|May 1, 1990
Dynamic left ventricular outflow obstruction after aortic valve replacement: a Doppler echocardiographic studyM E Schwinger, F O'Brien, R S Freedberg, et al.
European Archives of Psychiatry and Clinical Neuroscience|January 1, 1996
Eye tracking dysfunction in families with multiple cases of schizophreniaV Arolt, R Lencer, A Nolte, et al.
Klinische Monatsblatter Fur Augenheilkunde|June 1, 1992
[Bilateral colobomatous microphthalmus with orbital giant cysts in incomplete tetrasomy 22]W Lange, R Rochels, J Otte, et al.
HNO|August 1, 1996
[Familial occurrence of oculoauricolovertebral dysplasia and Franceschetti syndrome]U Bestelmeyer, H Weerda, R Siegert, et al.
Prenatal Diagnosis|January 13, 1999
Sonographically detected fetal and placental abnormalities associated with trisomy 16 confined to the placenta. A case report and review of the literatureA Astner, E Schwinger, A Caliebe, et al.
Journal of Neurology|July 7, 2005
Spinocerebellar ataxia type 4. Investigation of 34 candidate genesY Hellenbroich, H Pawlack, U Rüb, et al.
Pageof 22