Links to Exploration step
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Cleft hand/foot: clinical and developmental aspects.</title><author><name sortKey="Buss, P W" sort="Buss, P W" uniqKey="Buss P" first="P W" last="Buss">P W Buss</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">7815445</idno><idno type="pmc">1050086</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1050086</idno><idno type="RBID">PMC:1050086</idno><date when="1994">1994</date><idno type="wicri:Area/Pmc/Corpus">001891</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001891</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Cleft hand/foot: clinical and developmental aspects.</title><author><name sortKey="Buss, P W" sort="Buss, P W" uniqKey="Buss P" first="P W" last="Buss">P W Buss</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="1994">1994</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Isolated limb reduction defects occur in approximately 1 in 2000 live births within which central ray anomalies are an important subgroup. Most affected persons have mild or moderate functional impairment. Considerable psychological morbidity may also occur. While there have been major strides forwards in our understanding of vertebrate limb development, the mechanisms responsible for central ray deformities remain poorly understood. Several case reports of central clefting anomalies associated with chromosomal rearrangements or interstitial deletions of 7q21.2-q21.3 suggest that this chromosomal region is important for limb development.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><graphic xlink:href="jmedgene00288-0066-a" xlink:role="726"></graphic></fig><fig id="F2"><graphic xlink:href="jmedgene00288-0067-a" xlink:role="727"></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">7815445</article-id><article-id pub-id-type="pmc">1050086</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Cleft hand/foot: clinical and developmental aspects.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Buss</surname><given-names>P W</given-names></name></contrib></contrib-group><aff>Department of Neonatal Medicine, University of Bristol, UK.</aff><pub-date pub-type="ppub"><month>9</month><year>1994</year></pub-date><volume>31</volume><issue>9</issue><fpage>726</fpage><lpage>730</lpage><abstract><p>Isolated limb reduction defects occur in approximately 1 in 2000 live births within which central ray anomalies are an important subgroup. Most affected persons have mild or moderate functional impairment. Considerable psychological morbidity may also occur. While there have been major strides forwards in our understanding of vertebrate limb development, the mechanisms responsible for central ray deformities remain poorly understood. Several case reports of central clefting anomalies associated with chromosomal rearrangements or interstitial deletions of 7q21.2-q21.3 suggest that this chromosomal region is important for limb development.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><graphic xlink:href="jmedgene00288-0066-a" xlink:role="726"></graphic></fig><fig id="F2"><graphic xlink:href="jmedgene00288-0067-a" xlink:role="727"></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 001891 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 001891 | 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. |  |