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Clinical and genetic heterogeneity in autosomal dominant cataract.
Ionides A, Francis P, Berry V, Mackay D, Bhattacharya S, Shiels A, Moore A. Ionides A, et al. Among authors: shiels a. Br J Ophthalmol. 1999 Jul;83(7):802-8. doi: 10.1136/bjo.83.7.802. Br J Ophthalmol. 1999. PMID: 10381667 Free PMC article.
The clinical and genetic heterogeneity of autosomal dominant cataract.
Ionides A, Berry V, Moore T, Bhattacharya S, Shiels A. Ionides A, et al. Among authors: shiels a. Acta Ophthalmol Scand Suppl. 1996;(219):40-1. doi: 10.1111/j.1600-0420.1996.tb00383.x. Acta Ophthalmol Scand Suppl. 1996. PMID: 8741116 Review. No abstract available.
Connexin46 mutations in autosomal dominant congenital cataract.
Mackay D, Ionides A, Kibar Z, Rouleau G, Berry V, Moore A, Shiels A, Bhattacharya S. Mackay D, et al. Among authors: shiels a. Am J Hum Genet. 1999 May;64(5):1357-64. doi: 10.1086/302383. Am J Hum Genet. 1999. PMID: 10205266 Free PMC article.
Molecular mechanism underlying a Cx50-linked congenital cataract.
Pal JD, Berthoud VM, Beyer EC, Mackay D, Shiels A, Ebihara L. Pal JD, et al. Among authors: shiels a. Am J Physiol. 1999 Jun;276(6):C1443-6. doi: 10.1152/ajpcell.1999.276.6.C1443. Am J Physiol. 1999. PMID: 10362609
Mutations in gap junctional channels have been linked to certain forms of inherited congenital cataract (D. Mackay, A. Ionides, V. Berry, A. Moore, S. Bhattacharya, and A. Shiels. Am. J. Hum. Genet. 60: 1474-1478, 1997; A. Shiels, D. Mack …
Mutations in gap junctional channels have been linked to certain forms of inherited congenital cataract (D. Mackay, A. Ionides, V. Be …
112 results