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/Merge ); 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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<front><journal-meta><journal-id journal-id-type="nlm-ta">Trans Am Ophthalmol Soc</journal-id>
<journal-title>Transactions of the American Ophthalmological Society</journal-title>
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<article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject>
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<title-group><article-title>Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Lewis</surname>
<given-names>R A</given-names>
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<aff>Cullen Eye Institute, Baylor College of Medicine, Houston, TX.</aff>
<pub-date pub-type="ppub"><year>1989</year>
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<volume>87</volume>
<fpage>658</fpage>
<lpage>728</lpage>
<abstract abstract-type="scanned-figures"><sec sec-type="scanned-figures"><title>Images</title>
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