(Q48559934)

12 February 2018

title

2005 Gregg Lecture: Congenital cataract--from rubella to genetics (English)

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12 February 2018

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1

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12 February 2018

publication date

1 April 2006

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12 February 2018

Clinical and Experimental Ophthalmology

published in

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12 February 2018

volume

34

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12 February 2018

issue

3

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12 February 2018

page(s)

199-207

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12 February 2018

Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Aetiology of congenital and paediatric cataract in an Australian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Incidence and cumulative risk of childhood cataract in a cohort of 2.6 million Danish children

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Understanding the molecular genetics of congenital cataract may have wider implications for age related cataract

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Should we aggressively treat unilateral congenital cataracts?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Neonatal cataract: aetiology, pathogenesis and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Is early surgery for congenital cataract a risk factor for glaucoma?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Mutations in galactose-1-phosphate uridyltransferase gene in patients with idiopathic presenile cataract

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Nuclear cataract shows significant familial aggregation in an older population after adjustment for possible shared environmental factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Cortical, but not posterior subcapsular, cataract shows significant familial aggregation in an older population after adjustment for possible shared environmental factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Identification of a major locus for age-related cortical cataract on chromosome 6p12-q12 in the Beaver Dam Eye Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

Hereditary Hyperferritinemia-Cataract Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1442-9071.2006.01194.X

10.1111/J.1442-9071.2006.01194.X

21 January 2018

Identifiers

DOI

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12 February 2018

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12 February 2018