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Prenatal exclusion of Norrie disease with flanking DNA markers

✍ Scribed by Gal, Andreas ;Uhlhaas, Siegfried ;Glaser, Dieter ;Grimm, Tiemo ;Neri, Giovanni ;Reynolds, James F.

Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
316 KB
Volume
31
Category
Article
ISSN
0148-7299

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## Communicated by Mark H. Paalman Mutations at the Norrie disease gene locus, NDP, manifest in a broad range of defects. These range from a relatively mild, late-onset, exudative vitreoretinopathy to congenital blindness and sensorineural deafness combined, in some cases, with mental retardation.