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W Höpping

Showing results (11-20 of 23) with videos related to

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Human Genetics|October 1, 1994
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Human Genetics|July 1, 1987
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locusB Horsthemke, V Greger, H J Barnert, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1987
The prognosis of retinoblastoma in terms of globe saving treatment. A computer assisted study. Part IE de Sutter, W Havers, W Höpping, et al.
Journal of Medical Genetics|April 1, 1988
Application of linkage analysis to genetic counselling in families with hereditary retinoblastomaV Greger, S Kerst, E Messmer, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1984
Cavernous hemangioma of the retina. Immunohistochemical and ultrastructural observationsE Messmer, R L Font, H Laqua, et al.
Human Genetics|November 1, 1994
Frequency and parental origin of hypermethylated RB1 alleles in retinoblastomaV Greger, N Debus, D Lohmann, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 1, 1987
[Non-ocular, malignant secondary tumor following spontaneous healing of a retinoblastoma ("retinoma", "retinocytoma")]E P Messmer, H J Richter, W Höpping, et al.
Ophthalmology|February 1, 1991
Risk factors for metastases in patients with retinoblastomaE P Messmer, T Heinrich, W Höpping, et al.
Ophthalmic Genetics|December 1, 1995
Molecular analysis and predictive testing in retinoblastomaD R Lohmann, B Brandt, U Oehlschläger, et al.
American Journal of Medical Genetics|May 1, 1991
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaK Kloss, P Währisch, V Greger, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Human Genetics|October 1, 1994
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Human Genetics|July 1, 1987
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locusB Horsthemke, V Greger, H J Barnert, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1987
The prognosis of retinoblastoma in terms of globe saving treatment. A computer assisted study. Part IE de Sutter, W Havers, W Höpping, et al.
Journal of Medical Genetics|April 1, 1988
Application of linkage analysis to genetic counselling in families with hereditary retinoblastomaV Greger, S Kerst, E Messmer, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1984
Cavernous hemangioma of the retina. Immunohistochemical and ultrastructural observationsE Messmer, R L Font, H Laqua, et al.
Human Genetics|November 1, 1994
Frequency and parental origin of hypermethylated RB1 alleles in retinoblastomaV Greger, N Debus, D Lohmann, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 1, 1987
[Non-ocular, malignant secondary tumor following spontaneous healing of a retinoblastoma ("retinoma", "retinocytoma")]E P Messmer, H J Richter, W Höpping, et al.
Ophthalmology|February 1, 1991
Risk factors for metastases in patients with retinoblastomaE P Messmer, T Heinrich, W Höpping, et al.
Ophthalmic Genetics|December 1, 1995
Molecular analysis and predictive testing in retinoblastomaD R Lohmann, B Brandt, U Oehlschläger, et al.
American Journal of Medical Genetics|May 1, 1991
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaK Kloss, P Währisch, V Greger, et al.
Pageof 3