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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.</title>
<author><name sortKey="Pal, B" sort="Pal, B" uniqKey="Pal B" first="B" last="Pal">B. Pal</name>
</author>
<author><name sortKey="Mohamed, M" sort="Mohamed, M" uniqKey="Mohamed M" first="M" last="Mohamed">M. Mohamed</name>
</author>
<author><name sortKey="Keen, T" sort="Keen, T" uniqKey="Keen T" first="T" last="Keen">T. Keen</name>
</author>
<author><name sortKey="Williams, G" sort="Williams, G" uniqKey="Williams G" first="G" last="Williams">G. Williams</name>
</author>
<author><name sortKey="Bradbury, J" sort="Bradbury, J" uniqKey="Bradbury J" first="J" last="Bradbury">J. Bradbury</name>
</author>
<author><name sortKey="Sheridan, E" sort="Sheridan, E" uniqKey="Sheridan E" first="E" last="Sheridan">E. Sheridan</name>
</author>
<author><name sortKey="Inglehearn, C" sort="Inglehearn, C" uniqKey="Inglehearn C" first="C" last="Inglehearn">C. Inglehearn</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">15466012</idno>
<idno type="pmc">1735603</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735603</idno>
<idno type="RBID">PMC:1735603</idno>
<idno type="doi">10.1136/jmg.2004.020040</idno>
<date when="2004">2004</date>
<idno type="wicri:Area/Pmc/Corpus">004C26</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">004C26</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.</title>
<author><name sortKey="Pal, B" sort="Pal, B" uniqKey="Pal B" first="B" last="Pal">B. Pal</name>
</author>
<author><name sortKey="Mohamed, M" sort="Mohamed, M" uniqKey="Mohamed M" first="M" last="Mohamed">M. Mohamed</name>
</author>
<author><name sortKey="Keen, T" sort="Keen, T" uniqKey="Keen T" first="T" last="Keen">T. Keen</name>
</author>
<author><name sortKey="Williams, G" sort="Williams, G" uniqKey="Williams G" first="G" last="Williams">G. Williams</name>
</author>
<author><name sortKey="Bradbury, J" sort="Bradbury, J" uniqKey="Bradbury J" first="J" last="Bradbury">J. Bradbury</name>
</author>
<author><name sortKey="Sheridan, E" sort="Sheridan, E" uniqKey="Sheridan E" first="E" last="Sheridan">E. Sheridan</name>
</author>
<author><name sortKey="Inglehearn, C" sort="Inglehearn, C" uniqKey="Inglehearn C" first="C" last="Inglehearn">C. Inglehearn</name>
</author>
</analytic>
<series><title level="j">Journal of Medical Genetics</title>
<idno type="ISSN">0022-2593</idno>
<idno type="eISSN">1468-6244</idno>
<imprint><date when="2004">2004</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
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<profileDesc><textClass></textClass>
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<pmc xml:lang="EN" article-type="letter"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Med Genet</journal-id>
<journal-title>Journal of Medical Genetics</journal-title>
<issn pub-type="ppub">0022-2593</issn>
<issn pub-type="epub">1468-6244</issn>
<publisher><publisher-name>BMJ Group</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">15466012</article-id>
<article-id pub-id-type="pmc">1735603</article-id>
<article-id pub-id-type="doi">10.1136/jmg.2004.020040</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Letter to JMG</subject>
</subj-group>
</article-categories>
<title-group><article-title>A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Pal</surname>
<given-names>B</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Mohamed</surname>
<given-names>M</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Keen</surname>
<given-names>T</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Williams</surname>
<given-names>G</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Bradbury</surname>
<given-names>J</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Sheridan</surname>
<given-names>E</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Inglehearn</surname>
<given-names>C</given-names>
</name>
</contrib>
</contrib-group>
<pub-date pub-type="ppub"><month>10</month>
<year>2004</year>
</pub-date>
<volume>41</volume>
<issue>10</issue>
<fpage>772</fpage>
<lpage>777</lpage>
<self-uri xlink:role="pdf" xlink:type="simple" xlink:href="http://jmg.bmj.com/cgi/reprint/41/10/772.pdf"></self-uri>
<self-uri xlink:role="fulltext" xlink:type="simple" xlink:href="http://jmg.bmj.com/cgi/content/full/41/10/772"></self-uri>
</article-meta>
</front>
</pmc>
</record>
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