Author:
Meindl Alfons,Berger Wolfgang,Meitinger Thomas,van de Pol Dorien,Achatz Helene,Dörner Christa,Haasemann Martina,Hellebrand Heide,Gal Andreas,Cremers Frans,Ropers Hans-Hilger
Publisher
Springer Science and Business Media LLC
Reference40 articles.
1. Norrie, G. Causes of blindness in children. Acta Ophtalmol. 5, 357–386 (1927).
2. Warburg, M. Norrie's disease: A new hereditary bilateral pseudotumor of the retina. Acta Ophtalmol. 39, 757–772 (1961).
3. Warburg, M. Norrie's disease: A congenital progressive oculo-acoustico-cerebral degeneration. Acta Ophtalmol. 89, 1–147 (1966).
4. Gal, A., Wieringa, B., Smeets, D.F.C.M., Bleeker-Wagemakers, L.M. & Ropers, H.-H. Submicroscopic interstitial deletion of the X-chromosome explains a complex genetic syndrome dominated by Norrie disease. Cytogenet. Cell Genet. 42, 219–224 (1986).
5. Donnai, D., Mountford, R.C. & Read, A.P. Norrie disease resulting from a gene deletion clinical features and DNA studies. J. med. Genet. 25, 73–78 (1988).
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