Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature.
Identifieur interne : 008211 ( Ncbi/Merge ); précédent : 008210; suivant : 008212Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature.
Auteurs : Doris Milosavljevi [Pays-Bas] ; Eline Overwater [Pays-Bas] ; Saskia Tamminga [Pays-Bas] ; Karin De Boer [Pays-Bas] ; Mariet W. Elting [Pays-Bas] ; Marion E. Van Hoorn [Pays-Bas] ; Tuula Rinne [Pays-Bas] ; Arjan C. Houweling [Pays-Bas]Source :
- American journal of medical genetics. Part A [ 1552-4833 ] ; 2016.
Abstract
Mutations in RIT1, involved in the RAS-MAPK pathway, have recently been identified as a cause for Noonan syndrome. We present two patients with Noonan syndrome caused by a RIT1 mutation with novel phenotypic manifestations, severe bilateral lower limb lymphedema starting during puberty, and fetal hydrops resulting in intrauterine fetal death, respectively. Including our patients, a total of 52 patients have been reported with Noonan syndrome caused by a RIT1 mutation. Our report contributes to the delineation of the phenotype associated with RIT1 mutations and underlines that lymphatic involvement is part of this spectrum. In addition, we provide an overview of the currently described Noonan syndrome patients with RIT1 mutations in literature. © 2016 Wiley Periodicals, Inc.
DOI: 10.1002/ajmg.a.37657
PubMed: 27109146
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000861
- to stream PubMed, to step Curation: 000861
- to stream PubMed, to step Checkpoint: 000861
Links to Exploration step
pubmed:27109146Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature.</title>
<author><name sortKey="Milosavljevi, Doris" sort="Milosavljevi, Doris" uniqKey="Milosavljevi D" first="Doris" last="Milosavljevi">Doris Milosavljevi</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Overwater, Eline" sort="Overwater, Eline" uniqKey="Overwater E" first="Eline" last="Overwater">Eline Overwater</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Tamminga, Saskia" sort="Tamminga, Saskia" uniqKey="Tamminga S" first="Saskia" last="Tamminga">Saskia Tamminga</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="De Boer, Karin" sort="De Boer, Karin" uniqKey="De Boer K" first="Karin" last="De Boer">Karin De Boer</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Cardiology, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Cardiology, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Elting, Mariet W" sort="Elting, Mariet W" uniqKey="Elting M" first="Mariet W" last="Elting">Mariet W. Elting</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Van Hoorn, Marion E" sort="Van Hoorn, Marion E" uniqKey="Van Hoorn M" first="Marion E" last="Van Hoorn">Marion E. Van Hoorn</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Rinne, Tuula" sort="Rinne, Tuula" uniqKey="Rinne T" first="Tuula" last="Rinne">Tuula Rinne</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Human Genetics, Radboud University Medical Center, Nijmegen</wicri:regionArea>
<placeName><settlement type="city">Nimègue</settlement>
<region type="province" nuts="2">Gueldre</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Houweling, Arjan C" sort="Houweling, Arjan C" uniqKey="Houweling A" first="Arjan C" last="Houweling">Arjan C. Houweling</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2016">2016</date>
<idno type="RBID">pubmed:27109146</idno>
<idno type="pmid">27109146</idno>
<idno type="doi">10.1002/ajmg.a.37657</idno>
<idno type="wicri:Area/PubMed/Corpus">000861</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000861</idno>
<idno type="wicri:Area/PubMed/Curation">000861</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000861</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000861</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000861</idno>
<idno type="wicri:Area/Ncbi/Merge">008211</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature.</title>
<author><name sortKey="Milosavljevi, Doris" sort="Milosavljevi, Doris" uniqKey="Milosavljevi D" first="Doris" last="Milosavljevi">Doris Milosavljevi</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Overwater, Eline" sort="Overwater, Eline" uniqKey="Overwater E" first="Eline" last="Overwater">Eline Overwater</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Tamminga, Saskia" sort="Tamminga, Saskia" uniqKey="Tamminga S" first="Saskia" last="Tamminga">Saskia Tamminga</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="De Boer, Karin" sort="De Boer, Karin" uniqKey="De Boer K" first="Karin" last="De Boer">Karin De Boer</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Cardiology, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Cardiology, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Elting, Mariet W" sort="Elting, Mariet W" uniqKey="Elting M" first="Mariet W" last="Elting">Mariet W. Elting</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Van Hoorn, Marion E" sort="Van Hoorn, Marion E" uniqKey="Van Hoorn M" first="Marion E" last="Van Hoorn">Marion E. Van Hoorn</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Rinne, Tuula" sort="Rinne, Tuula" uniqKey="Rinne T" first="Tuula" last="Rinne">Tuula Rinne</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Human Genetics, Radboud University Medical Center, Nijmegen</wicri:regionArea>
<placeName><settlement type="city">Nimègue</settlement>
<region type="province" nuts="2">Gueldre</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Houweling, Arjan C" sort="Houweling, Arjan C" uniqKey="Houweling A" first="Arjan C" last="Houweling">Arjan C. Houweling</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Clinical Genetics, VU University Medical Center, Amsterdam</wicri:regionArea>
<placeName><settlement type="city">Amsterdam</settlement>
<region nuts="2" type="province">Hollande-Septentrionale</region>
</placeName>
</affiliation>
</author>
</analytic>
<series><title level="j">American journal of medical genetics. Part A</title>
<idno type="eISSN">1552-4833</idno>
<imprint><date when="2016" type="published">2016</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Mutations in RIT1, involved in the RAS-MAPK pathway, have recently been identified as a cause for Noonan syndrome. We present two patients with Noonan syndrome caused by a RIT1 mutation with novel phenotypic manifestations, severe bilateral lower limb lymphedema starting during puberty, and fetal hydrops resulting in intrauterine fetal death, respectively. Including our patients, a total of 52 patients have been reported with Noonan syndrome caused by a RIT1 mutation. Our report contributes to the delineation of the phenotype associated with RIT1 mutations and underlines that lymphatic involvement is part of this spectrum. In addition, we provide an overview of the currently described Noonan syndrome patients with RIT1 mutations in literature. © 2016 Wiley Periodicals, Inc.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="In-Process" Owner="NLM"><PMID Version="1">27109146</PMID>
<DateCreated><Year>2016</Year>
<Month>06</Month>
<Day>17</Day>
</DateCreated>
<DateRevised><Year>2016</Year>
<Month>06</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1552-4833</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>170</Volume>
<Issue>7</Issue>
<PubDate><Year>2016</Year>
<Month>Jul</Month>
</PubDate>
</JournalIssue>
<Title>American journal of medical genetics. Part A</Title>
<ISOAbbreviation>Am. J. Med. Genet. A</ISOAbbreviation>
</Journal>
<ArticleTitle>Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature.</ArticleTitle>
<Pagination><MedlinePgn>1874-80</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/ajmg.a.37657</ELocationID>
<Abstract><AbstractText>Mutations in RIT1, involved in the RAS-MAPK pathway, have recently been identified as a cause for Noonan syndrome. We present two patients with Noonan syndrome caused by a RIT1 mutation with novel phenotypic manifestations, severe bilateral lower limb lymphedema starting during puberty, and fetal hydrops resulting in intrauterine fetal death, respectively. Including our patients, a total of 52 patients have been reported with Noonan syndrome caused by a RIT1 mutation. Our report contributes to the delineation of the phenotype associated with RIT1 mutations and underlines that lymphatic involvement is part of this spectrum. In addition, we provide an overview of the currently described Noonan syndrome patients with RIT1 mutations in literature. © 2016 Wiley Periodicals, Inc.</AbstractText>
<CopyrightInformation>© 2016 Wiley Periodicals, Inc.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Milosavljević</LastName>
<ForeName>Doris</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Experimental Cardiology, Academic Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Overwater</LastName>
<ForeName>Eline</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Tamminga</LastName>
<ForeName>Saskia</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>de Boer</LastName>
<ForeName>Karin</ForeName>
<Initials>K</Initials>
<AffiliationInfo><Affiliation>Department of Cardiology, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Elting</LastName>
<ForeName>Mariet W</ForeName>
<Initials>MW</Initials>
<AffiliationInfo><Affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>van Hoorn</LastName>
<ForeName>Marion E</ForeName>
<Initials>ME</Initials>
<AffiliationInfo><Affiliation>Department of Obstetrics and Gynecology, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Rinne</LastName>
<ForeName>Tuula</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Houweling</LastName>
<ForeName>Arjan C</ForeName>
<Initials>AC</Initials>
<AffiliationInfo><Affiliation>Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2016</Year>
<Month>04</Month>
<Day>25</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Am J Med Genet A</MedlineTA>
<NlmUniqueID>101235741</NlmUniqueID>
<ISSNLinking>1552-4825</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Noonan syndrome</Keyword>
<Keyword MajorTopicYN="N">RASopathy</Keyword>
<Keyword MajorTopicYN="N">RIT1</Keyword>
<Keyword MajorTopicYN="N">hydrops fetalis</Keyword>
<Keyword MajorTopicYN="N">lymphedema</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year>
<Month>01</Month>
<Day>14</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2016</Year>
<Month>03</Month>
<Day>20</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2016</Year>
<Month>4</Month>
<Day>26</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2016</Year>
<Month>4</Month>
<Day>26</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2016</Year>
<Month>4</Month>
<Day>26</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">27109146</ArticleId>
<ArticleId IdType="doi">10.1002/ajmg.a.37657</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>Pays-Bas</li>
</country>
<region><li>Gueldre</li>
<li>Hollande-Septentrionale</li>
</region>
<settlement><li>Amsterdam</li>
<li>Nimègue</li>
</settlement>
</list>
<tree><country name="Pays-Bas"><region name="Hollande-Septentrionale"><name sortKey="Milosavljevi, Doris" sort="Milosavljevi, Doris" uniqKey="Milosavljevi D" first="Doris" last="Milosavljevi">Doris Milosavljevi</name>
</region>
<name sortKey="De Boer, Karin" sort="De Boer, Karin" uniqKey="De Boer K" first="Karin" last="De Boer">Karin De Boer</name>
<name sortKey="Elting, Mariet W" sort="Elting, Mariet W" uniqKey="Elting M" first="Mariet W" last="Elting">Mariet W. Elting</name>
<name sortKey="Houweling, Arjan C" sort="Houweling, Arjan C" uniqKey="Houweling A" first="Arjan C" last="Houweling">Arjan C. Houweling</name>
<name sortKey="Overwater, Eline" sort="Overwater, Eline" uniqKey="Overwater E" first="Eline" last="Overwater">Eline Overwater</name>
<name sortKey="Rinne, Tuula" sort="Rinne, Tuula" uniqKey="Rinne T" first="Tuula" last="Rinne">Tuula Rinne</name>
<name sortKey="Tamminga, Saskia" sort="Tamminga, Saskia" uniqKey="Tamminga S" first="Saskia" last="Tamminga">Saskia Tamminga</name>
<name sortKey="Van Hoorn, Marion E" sort="Van Hoorn, Marion E" uniqKey="Van Hoorn M" first="Marion E" last="Van Hoorn">Marion E. Van Hoorn</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Ncbi/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 008211 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 008211 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= Ncbi |étape= Merge |type= RBID |clé= pubmed:27109146 |texte= Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i -Sk "pubmed:27109146" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd \ | NlmPubMed2Wicri -a LymphedemaV1
![]() | This area was generated with Dilib version V0.6.31. | ![]() |