Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

Author:

Wolff G,Mayerova A,Wienker T F,Atalianis P,Ioannou P,Warburg M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. Norrie's disease: a new hereditary bilateral pseudotumor of the retina;Warburg, M.;Acta Ophthalmol (Copenh)

2. Norrie's disease, a congenital progressive oculo-acustico-cerebral degeneration;Warburg, M.;Acta Ophthalmol (Copenh),1966

3. Audiological findings in Norrie's disease;Parving, A.; Warburg, M.;Audiology,1977

4. Norrie's disease;Johnston, S.S.; Hanna, J.E.; Nevin, N.C.; Bryars, J.H.;Birth Defects,1982

5. Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosome;Gal, A.; Stolzenberger, C.; Wienker, T.;Clin Genet,1985

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1. Inherited causes of combined vision and hearing loss: clinical features and molecular genetics;British Journal of Ophthalmology;2022-09-26

2. B-Cell Receptor-Associated Protein 31 Negatively Regulates the Expression of Monoamine Oxidase A Via R1;Frontiers in Molecular Biosciences;2020-04-30

3. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

4. If only you do it well Autobiography;Ophthalmic Genetics;1996-01

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