Links to Exploration step
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0).</title>
<author><name sortKey="Watt, J L" sort="Watt, J L" uniqKey="Watt J" first="J L" last="Watt">J L Watt</name>
</author>
<author><name sortKey="Couzin, D A" sort="Couzin, D A" uniqKey="Couzin D" first="D A" last="Couzin">D A Couzin</name>
</author>
<author><name sortKey="Johnston, A W" sort="Johnston, A W" uniqKey="Johnston A" first="A W" last="Johnston">A W Johnston</name>
</author>
<author><name sortKey="Jandial, V" sort="Jandial, V" uniqKey="Jandial V" first="V" last="Jandial">V. Jandial</name>
</author>
<author><name sortKey="Gray, E S" sort="Gray, E S" uniqKey="Gray E" first="E S" last="Gray">E S Gray</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">7241546</idno>
<idno type="pmc">1048710</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1048710</idno>
<idno type="RBID">PMC:1048710</idno>
<date when="1981">1981</date>
<idno type="wicri:Area/Pmc/Corpus">001890</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001890</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0).</title>
<author><name sortKey="Watt, J L" sort="Watt, J L" uniqKey="Watt J" first="J L" last="Watt">J L Watt</name>
</author>
<author><name sortKey="Couzin, D A" sort="Couzin, D A" uniqKey="Couzin D" first="D A" last="Couzin">D A Couzin</name>
</author>
<author><name sortKey="Johnston, A W" sort="Johnston, A W" uniqKey="Johnston A" first="A W" last="Johnston">A W Johnston</name>
</author>
<author><name sortKey="Jandial, V" sort="Jandial, V" uniqKey="Jandial V" first="V" last="Jandial">V. Jandial</name>
</author>
<author><name sortKey="Gray, E S" sort="Gray, E S" uniqKey="Gray E" first="E S" last="Gray">E S Gray</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="1981">1981</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>A case of Turner's syndrome, detected antenatally and complicated by the finding of trisomy 20 mosaicism in 50% of cells from each of two amniotic fluid cultures, is described. Cultures from seven fetal tissues in the subsequent abortus showed a predominance of 45,X cells, but nevertheless suggested the existence of a very low level of trisomy 20 mosaicism in three fetal tissues. The diagnostic dilemma in interpreting trisomy 20 mosaicism is discussed.</p>
<sec sec-type="scanned-figures"><title>Images</title>
<fig id="F1"><graphic xlink:href="jmedgene00119-0068-a" xlink:role="226"></graphic>
</fig>
<fig id="F2"><graphic xlink:href="jmedgene00119-0068-b" xlink:role="226"></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">7241546</article-id>
<article-id pub-id-type="pmc">1048710</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0).</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Watt</surname>
<given-names>J L</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Couzin</surname>
<given-names>D A</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Johnston</surname>
<given-names>A W</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Jandial</surname>
<given-names>V</given-names>
</name>
</contrib>
<contrib contrib-type="author"><name><surname>Gray</surname>
<given-names>E S</given-names>
</name>
</contrib>
</contrib-group>
<pub-date pub-type="ppub"><month>6</month>
<year>1981</year>
</pub-date>
<volume>18</volume>
<issue>3</issue>
<fpage>225</fpage>
<lpage>227</lpage>
<abstract><p>A case of Turner's syndrome, detected antenatally and complicated by the finding of trisomy 20 mosaicism in 50% of cells from each of two amniotic fluid cultures, is described. Cultures from seven fetal tissues in the subsequent abortus showed a predominance of 45,X cells, but nevertheless suggested the existence of a very low level of trisomy 20 mosaicism in three fetal tissues. The diagnostic dilemma in interpreting trisomy 20 mosaicism is discussed.</p>
<sec sec-type="scanned-figures"><title>Images</title>
<fig id="F1"><graphic xlink:href="jmedgene00119-0068-a" xlink:role="226"></graphic>
</fig>
<fig id="F2"><graphic xlink:href="jmedgene00119-0068-b" xlink:role="226"></graphic>
</fig>
</sec>
</abstract>
</article-meta>
</front>
</pmc>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 0018909 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 0018909 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= Pmc |étape= Corpus |type= RBID |clé= |texte= }}
![]() | This area was generated with Dilib version V0.6.31. | ![]() |