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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 : 001834 ( Pmc/Curation ); précédent : 001833; suivant : 001835

Mapping 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 Lewis

Source :

Transactions of the American Ophthalmological Society [ 0065-9533 ] ; 1989.

RBID : PMC:1298561

Abstract

ImagesFIGURE 4 AFIGURE 4 BFIGURE 4 CFIGURE 4 DFIGURE 4 EFIGURE 4 FFIGURE 4 GFIGURE 4 HFIGURE 6 AFIGURE 6 BFIGURE 6 CFIGURE 6 DFIGURE 6 EFIGURE 6 FFIGURE 6 GFIGURE 6 HFIGURE 8 AFIGURE 8 BFIGURE 8 CFIGURE 8 DFIGURE 8 EFIGURE 8 FFIGURE 10 AFIGURE 10 BFIGURE 10 CFIGURE 10 DFIGURE 10 EFIGURE 10 FFIGURE 12 AFIGURE 12 BFIGURE 12 DFIGURE 12 C

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1298561

PubMed: 2576480
PubMed Central: 1298561

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PMC:1298561

Le document en format XML

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  <front><journal-meta><journal-id journal-id-type="nlm-ta">Trans Am Ophthalmol Soc</journal-id>
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<contrib-group><contrib contrib-type="author"><name><surname>Lewis</surname>
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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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Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

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Abstract

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