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Author/Creator Reddy, M A

1. A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma. Issue 2 (1st February 2003)

Authors:
Reddy, M A; Francis, P J; Berry, V; Bradshaw, K; Patel, R J; Maher, E R; Kumar, R; Bhattacharya, S S; Moore, A T
Journal:
British journal of ophthalmology
Issue:
Volume 87:Issue 2(2003)
Page Start:
197
Record Type:
Journal Article
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2. A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract. Issue 1 (5th January 2006)

Authors:
Arora, A; Minogue, P J; Liu, X; Reddy, M A; Ainsworth, J R; Bhattacharya, S S; Webster, A R; Hunt, D M; Ebihara, L; Moore, A T; Beyer, E C; Berthoud, V M
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 1(2006)
Page Start:
e2
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗