Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence
Identifieur interne : 00E831 ( Main/Exploration ); précédent : 00E830; suivant : 00E832Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence
Auteurs : Alexander K. C. Leung [Canada] ; John M. OpitzSource :
- American Journal of Medical Genetics [ 0148-7299 ] ; 1987-01.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Lymphoedème, Malformations multiples, Microcéphalie.
- psychologie : Malformations multiples, Microcéphalie.
- Gènes dominants, Humains, Intelligence, Lymphoedème, Syndrome.
English descriptors
- KwdEn :
- MESH :
- congenital : Lymphedema.
- genetics : Abnormalities, Multiple, Lymphedema, Microcephaly.
- psychology : Abnormalities, Multiple, Microcephaly.
- Genes, Dominant, Humans, Intelligence, Syndrome.
Url:
DOI: 10.1002/ajmg.1320260136
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 006584
- to stream Istex, to step Curation: 006584
- to stream Istex, to step Checkpoint: 005C08
- to stream PubMed, to step Corpus: 006435
- to stream PubMed, to step Curation: 006435
- to stream PubMed, to step Checkpoint: 006435
- to stream Ncbi, to step Merge: 009A85
- to stream Ncbi, to step Curation: 009A85
- to stream Ncbi, to step Checkpoint: 009A85
- to stream Main, to step Merge: 00F554
- to stream Main, to step Curation: 00E831
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence</title>
<author><name sortKey="Leung, Alexander K C" sort="Leung, Alexander K C" uniqKey="Leung A" first="Alexander K. C." last="Leung">Alexander K. C. Leung</name>
</author>
<author><name sortKey="Opitz, John M" sort="Opitz, John M" uniqKey="Opitz J" first="John M." last="Opitz">John M. Opitz</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:D8FC57042AB6881E5B5675A7CFA87E4D587ADCAB</idno>
<date when="1987" year="1987">1987</date>
<idno type="doi">10.1002/ajmg.1320260136</idno>
<idno type="url">https://api.istex.fr/document/D8FC57042AB6881E5B5675A7CFA87E4D587ADCAB/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">006584</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">006584</idno>
<idno type="wicri:Area/Istex/Curation">006584</idno>
<idno type="wicri:Area/Istex/Checkpoint">005C08</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">005C08</idno>
<idno type="wicri:doubleKey">0148-7299:1987:Leung A:dominantly:inherited:syndrome</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:3812569</idno>
<idno type="wicri:Area/PubMed/Corpus">006435</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">006435</idno>
<idno type="wicri:Area/PubMed/Curation">006435</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">006435</idno>
<idno type="wicri:Area/PubMed/Checkpoint">006435</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">006435</idno>
<idno type="wicri:Area/Ncbi/Merge">009A85</idno>
<idno type="wicri:Area/Ncbi/Curation">009A85</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">009A85</idno>
<idno type="wicri:doubleKey">0148-7299:1987:Leung A:dominantly:inherited:syndrome</idno>
<idno type="wicri:Area/Main/Merge">00F554</idno>
<idno type="wicri:Area/Main/Curation">00E831</idno>
<idno type="wicri:Area/Main/Exploration">00E831</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence</title>
<author><name sortKey="Leung, Alexander K C" sort="Leung, Alexander K C" uniqKey="Leung A" first="Alexander K. C." last="Leung">Alexander K. C. Leung</name>
<affiliation wicri:level="4"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Pediatrics, University of Calgary, Alberta Children's Hospital, Calgary, Alberta</wicri:regionArea>
<orgName type="university">Université de Calgary</orgName>
<placeName><settlement type="city">Calgary</settlement>
<region type="state">Alberta</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Opitz, John M" sort="Opitz, John M" uniqKey="Opitz J" first="John M." last="Opitz">John M. Opitz</name>
</author>
</analytic>
<monogr></monogr>
<series><title level="j" type="main">American Journal of Medical Genetics</title>
<title level="j" type="alt">AMERICAN JOURNAL OF MEDICAL GENETICS</title>
<idno type="ISSN">0148-7299</idno>
<idno type="eISSN">1096-8628</idno>
<imprint><biblScope unit="vol">26</biblScope>
<biblScope unit="issue">1</biblScope>
<biblScope unit="page" from="231">231</biblScope>
<biblScope unit="page" to="231">231</biblScope>
<biblScope unit="page-count">1</biblScope>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>New York</pubPlace>
<date type="published" when="1987-01">1987-01</date>
</imprint>
<idno type="ISSN">0148-7299</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0148-7299</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abnormalities, Multiple (genetics)</term>
<term>Abnormalities, Multiple (psychology)</term>
<term>Genes, Dominant</term>
<term>Humans</term>
<term>Intelligence</term>
<term>Lymphedema (congenital)</term>
<term>Lymphedema (genetics)</term>
<term>Microcephaly (genetics)</term>
<term>Microcephaly (psychology)</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Gènes dominants</term>
<term>Humains</term>
<term>Intelligence</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (génétique)</term>
<term>Malformations multiples (génétique)</term>
<term>Malformations multiples (psychologie)</term>
<term>Microcéphalie (génétique)</term>
<term>Microcéphalie (psychologie)</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Abnormalities, Multiple</term>
<term>Lymphedema</term>
<term>Microcephaly</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lymphoedème</term>
<term>Malformations multiples</term>
<term>Microcéphalie</term>
</keywords>
<keywords scheme="MESH" qualifier="psychologie" xml:lang="fr"><term>Malformations multiples</term>
<term>Microcéphalie</term>
</keywords>
<keywords scheme="MESH" qualifier="psychology" xml:lang="en"><term>Abnormalities, Multiple</term>
<term>Microcephaly</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Genes, Dominant</term>
<term>Humans</term>
<term>Intelligence</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Gènes dominants</term>
<term>Humains</term>
<term>Intelligence</term>
<term>Lymphoedème</term>
<term>Syndrome</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list><country><li>Canada</li>
</country>
<region><li>Alberta</li>
</region>
<settlement><li>Calgary</li>
</settlement>
<orgName><li>Université de Calgary</li>
</orgName>
</list>
<tree><noCountry><name sortKey="Opitz, John M" sort="Opitz, John M" uniqKey="Opitz J" first="John M." last="Opitz">John M. Opitz</name>
</noCountry>
<country name="Canada"><region name="Alberta"><name sortKey="Leung, Alexander K C" sort="Leung, Alexander K C" uniqKey="Leung A" first="Alexander K. C." last="Leung">Alexander K. C. Leung</name>
</region>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 00E831 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 00E831 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:D8FC57042AB6881E5B5675A7CFA87E4D587ADCAB |texte= Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence }}
This area was generated with Dilib version V0.6.31. |