Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.
Identifieur interne : 005939 ( Ncbi/Curation ); précédent : 005938; suivant : 005940Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.
Auteurs : R A LewisSource :
- Transactions of the American Ophthalmological Society [ 0065-9533 ] ; 1989.
Abstract
Url:
PubMed: 2576480
PubMed Central: 1298561
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PMC:1298561Le document en format XML
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<front><div type="abstract" xml:lang="en"><sec sec-type="scanned-figures"><title>Images</title>
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