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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma</title><author><name sortKey="Hienonen, T" sort="Hienonen, T" uniqKey="Hienonen T" first="T" last="Hienonen">T. Hienonen</name></author><author><name sortKey="Sammalkorpi, H" sort="Sammalkorpi, H" uniqKey="Sammalkorpi H" first="H" last="Sammalkorpi">H. Sammalkorpi</name></author><author><name sortKey="Isohanni, P" sort="Isohanni, P" uniqKey="Isohanni P" first="P" last="Isohanni">P. Isohanni</name></author><author><name sortKey="Versteeg, R" sort="Versteeg, R" uniqKey="Versteeg R" first="R" last="Versteeg">R. Versteeg</name></author><author><name sortKey="Karikoski, R" sort="Karikoski, R" uniqKey="Karikoski R" first="R" last="Karikoski">R. Karikoski</name></author><author><name sortKey="Aaltonen, L" sort="Aaltonen, L" uniqKey="Aaltonen L" first="L" last="Aaltonen">L. Aaltonen</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">15635065</idno><idno type="pmc">1735919</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735919</idno><idno type="RBID">PMC:1735919</idno><idno type="doi">10.1136/jmg.2004.022814</idno><date when="2005">2005</date><idno type="wicri:Area/Pmc/Corpus">000220</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000220</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma</title><author><name sortKey="Hienonen, T" sort="Hienonen, T" uniqKey="Hienonen T" first="T" last="Hienonen">T. Hienonen</name></author><author><name sortKey="Sammalkorpi, H" sort="Sammalkorpi, H" uniqKey="Sammalkorpi H" first="H" last="Sammalkorpi">H. Sammalkorpi</name></author><author><name sortKey="Isohanni, P" sort="Isohanni, P" uniqKey="Isohanni P" first="P" last="Isohanni">P. Isohanni</name></author><author><name sortKey="Versteeg, R" sort="Versteeg, R" uniqKey="Versteeg R" first="R" last="Versteeg">R. Versteeg</name></author><author><name sortKey="Karikoski, R" sort="Karikoski, R" uniqKey="Karikoski R" first="R" last="Karikoski">R. Karikoski</name></author><author><name sortKey="Aaltonen, L" sort="Aaltonen, L" uniqKey="Aaltonen L" first="L" last="Aaltonen">L. Aaltonen</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="2005">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader></TEI><pmc xml:lang="EN" article-type="case-report"><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">15635065</article-id><article-id pub-id-type="pmc">1735919</article-id><article-id pub-id-type="doi">10.1136/jmg.2004.022814</article-id><article-categories><subj-group subj-group-type="heading"><subject>Online Mutation Report</subject></subj-group></article-categories><title-group><article-title>A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Hienonen</surname><given-names>T</given-names></name></contrib><contrib contrib-type="author"><name><surname>Sammalkorpi</surname><given-names>H</given-names></name></contrib><contrib contrib-type="author"><name><surname>Isohanni</surname><given-names>P</given-names></name></contrib><contrib contrib-type="author"><name><surname>Versteeg</surname><given-names>R</given-names></name></contrib><contrib contrib-type="author"><name><surname>Karikoski</surname><given-names>R</given-names></name></contrib><contrib contrib-type="author"><name><surname>Aaltonen</surname><given-names>L</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><month>1</month><year>2005</year></pub-date><volume>42</volume><issue>1</issue><fpage>e3</fpage><lpage>e3</lpage><self-uri xlink:role="pdf" xlink:type="simple" xlink:href="http://jmg.bmj.com/cgi/reprint/42/1/e3.pdf"></self-uri><self-uri xlink:role="fulltext" xlink:type="simple" xlink:href="http://jmg.bmj.com/cgi/content/full/42/1/e3"></self-uri></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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