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Autosomal dominant brachydactyly, coloboma and anterior segment dysgenesis.

Quinn S, Black GCM, Biswas S, Clayton-Smith J, Lloyd I

Ophthalmic Genet. 2004;25( 4):277-83.

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Abstract

A three-generation family presenting with ocular developmental abnormalities, including anterior segment dysgenesis and coloboma, associated with brachydactyly and clinodactyly is presented. Several conditions incorporating ocular and bony limb abnormalities have been described. However, we believe that this family manifests a previously undescribed syndrome due to autosomal dominant or possibly x-linked inheritance with variable expression.

Bibliographic metadata

Type of resource:
Content type:
Publication type:
Publication form:
Published date:
Journal title:
ISSN:
Place of publication:
Netherlands
Volume:
25( 4)
Start page:
277
End page:
83
Pagination:
277-83
Access state:
Active

Institutional metadata

University researcher(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:1d10672
Created:
29th August, 2009, 15:41:52
Last modified:
15th April, 2014, 12:58:44

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