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Article

Phenotypic variation in ophthalmic manifestations of MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea).

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Jul 2004

Cape Catherine J, Zaidman Gerald W, Beck Allen D, Kaufman Adam H

Abstract excerpt

No abstract is available from the source.

Topics

Chromosome Deletion
Chromosomes, Human, X
Corneal Diseases
Diseases in Twins
Ectodermal Dysplasia
Female
Humans
Infant, Newborn
Male
Microphthalmos
Phenotype
Scleral Diseases
Syndrome

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Source

Identifiers

PMID: 15249380
DOI: 10.1001/archopht.122.7.1070

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