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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">45,X Turner's syndrome in monozygotic twin sisters.</title><author><name sortKey="Pescia, G" sort="Pescia, G" uniqKey="Pescia G" first="G" last="Pescia">G. Pescia</name></author><author><name sortKey="Ferrier, P E" sort="Ferrier, P E" uniqKey="Ferrier P" first="P E" last="Ferrier">P E Ferrier</name></author><author><name sortKey="Wyss Hutin, D" sort="Wyss Hutin, D" uniqKey="Wyss Hutin D" first="D" last="Wyss-Hutin">D. Wyss-Hutin</name></author><author><name sortKey="Klein, D" sort="Klein, D" uniqKey="Klein D" first="D" last="Klein">D. Klein</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">1240972</idno><idno type="pmc">1013318</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1013318</idno><idno type="RBID">PMC:1013318</idno><date when="1975">1975</date><idno type="wicri:Area/Pmc/Corpus">001862</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001862</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">45,X Turner's syndrome in monozygotic twin sisters.</title><author><name sortKey="Pescia, G" sort="Pescia, G" uniqKey="Pescia G" first="G" last="Pescia">G. Pescia</name></author><author><name sortKey="Ferrier, P E" sort="Ferrier, P E" uniqKey="Ferrier P" first="P E" last="Ferrier">P E Ferrier</name></author><author><name sortKey="Wyss Hutin, D" sort="Wyss Hutin, D" uniqKey="Wyss Hutin D" first="D" last="Wyss-Hutin">D. Wyss-Hutin</name></author><author><name sortKey="Klein, D" sort="Klein, D" uniqKey="Klein D" first="D" last="Klein">D. Klein</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="1975">1975</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>A 7-year-old girl was admitted to the hospital for anaemia, secondary to intestinal blood los (melaena). She was found to have 45,X Turner's syndrome. Her identical twin sister also had Turner's syndrome with a 45,X chromosome complement. According to various criteria the probability of monozygosity was 0.9905. Although the incidence of twinning is greater than usual in families of patients with Turner's syndrome, affected cases have only been observed in twin sisters on six occasions. It seems therefore that the 45,X chromosome complement itself is not a factor predisposing to twinning, but that in some families, a factor is at play, which cuases either twinning or the 45,X aneuploidy, or both.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><graphic xlink:href="jmedgene00317-0075-a" xlink:role="391"></graphic></fig><fig id="F2"><graphic xlink:href="jmedgene00317-0075-b" xlink:role="391"></graphic></fig><fig id="F3"><graphic xlink:href="jmedgene00317-0076-a" xlink:role="392"></graphic></fig></sec></div></front></TEI><pmc article-type="research-article"><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></journal-meta><article-meta><article-id pub-id-type="pmid">1240972</article-id><article-id pub-id-type="pmc">1013318</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>45,X Turner's syndrome in monozygotic twin sisters.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Pescia</surname><given-names>G</given-names></name></contrib><contrib contrib-type="author"><name><surname>Ferrier</surname><given-names>P E</given-names></name></contrib><contrib contrib-type="author"><name><surname>Wyss-Hutin</surname><given-names>D</given-names></name></contrib><contrib contrib-type="author"><name><surname>Klein</surname><given-names>D</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><month>12</month><year>1975</year></pub-date><volume>12</volume><issue>4</issue><fpage>390</fpage><lpage>396</lpage><abstract><p>A 7-year-old girl was admitted to the hospital for anaemia, secondary to intestinal blood los (melaena). She was found to have 45,X Turner's syndrome. Her identical twin sister also had Turner's syndrome with a 45,X chromosome complement. According to various criteria the probability of monozygosity was 0.9905. Although the incidence of twinning is greater than usual in families of patients with Turner's syndrome, affected cases have only been observed in twin sisters on six occasions. It seems therefore that the 45,X chromosome complement itself is not a factor predisposing to twinning, but that in some families, a factor is at play, which cuases either twinning or the 45,X aneuploidy, or both.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><graphic xlink:href="jmedgene00317-0075-a" xlink:role="391"></graphic></fig><fig id="F2"><graphic xlink:href="jmedgene00317-0075-b" xlink:role="391"></graphic></fig><fig id="F3"><graphic xlink:href="jmedgene00317-0076-a" xlink:role="392"></graphic></fig></sec></abstract></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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