An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier
Identifieur interne : 007032 ( Main/Merge ); précédent : 007031; suivant : 007033An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier
Auteurs : Tanya L. Gillan [Canada] ; Christine Davies [Canada] ; A. Micheil Innes [Canada] ; Jayda Howard [Canada] ; Lisa Graham [Canada] ; Judy Chernos [Canada] ; Peter J. Bridge [Canada] ; Jillian S. Parboosingh [Canada]Source :
- American Journal of Medical Genetics Part A [ 1552-4825 ] ; 2008-04-15.
Url:
DOI: 10.1002/ajmg.a.32231
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 004E40
- to stream Istex, to step Curation: 004E40
- to stream Istex, to step Checkpoint: 001182
Links to Exploration step
ISTEX:A6AE0FA77B39EB44407CAAC30CB96A9E85714668Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier</title>
<author><name sortKey="Gillan, Tanya L" sort="Gillan, Tanya L" uniqKey="Gillan T" first="Tanya L." last="Gillan">Tanya L. Gillan</name>
</author>
<author><name sortKey="Davies, Christine" sort="Davies, Christine" uniqKey="Davies C" first="Christine" last="Davies">Christine Davies</name>
</author>
<author><name sortKey="Innes, A Micheil" sort="Innes, A Micheil" uniqKey="Innes A" first="A. Micheil" last="Innes">A. Micheil Innes</name>
</author>
<author><name sortKey="Howard, Jayda" sort="Howard, Jayda" uniqKey="Howard J" first="Jayda" last="Howard">Jayda Howard</name>
</author>
<author><name sortKey="Graham, Lisa" sort="Graham, Lisa" uniqKey="Graham L" first="Lisa" last="Graham">Lisa Graham</name>
</author>
<author><name sortKey="Chernos, Judy" sort="Chernos, Judy" uniqKey="Chernos J" first="Judy" last="Chernos">Judy Chernos</name>
</author>
<author><name sortKey="Bridge, Peter J" sort="Bridge, Peter J" uniqKey="Bridge P" first="Peter J." last="Bridge">Peter J. Bridge</name>
</author>
<author><name sortKey="Parboosingh, Jillian S" sort="Parboosingh, Jillian S" uniqKey="Parboosingh J" first="Jillian S." last="Parboosingh">Jillian S. Parboosingh</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:A6AE0FA77B39EB44407CAAC30CB96A9E85714668</idno>
<date when="2008" year="2008">2008</date>
<idno type="doi">10.1002/ajmg.a.32231</idno>
<idno type="url">https://api.istex.fr/document/A6AE0FA77B39EB44407CAAC30CB96A9E85714668/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">004E40</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">004E40</idno>
<idno type="wicri:Area/Istex/Curation">004E40</idno>
<idno type="wicri:Area/Istex/Checkpoint">001182</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001182</idno>
<idno type="wicri:doubleKey">1552-4825:2008:Gillan T:an:undiagnosed:cytogenetic</idno>
<idno type="wicri:Area/Main/Merge">007032</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier<ref type="note" target="#fn1"></ref>
<ref type="note" target="#fn2"></ref>
</title>
<author><name sortKey="Gillan, Tanya L" sort="Gillan, Tanya L" uniqKey="Gillan T" first="Tanya L." last="Gillan">Tanya L. Gillan</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Molecular Diagnostic Laboratory, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Davies, Christine" sort="Davies, Christine" uniqKey="Davies C" first="Christine" last="Davies">Christine Davies</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Clinical Genetics Unit, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Innes, A Micheil" sort="Innes, A Micheil" uniqKey="Innes A" first="A. Micheil" last="Innes">A. Micheil Innes</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Clinical Genetics Unit, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
<affiliation wicri:level="4"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Medical Genetics, University of Calgary, Calgary</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="Howard, Jayda" sort="Howard, Jayda" uniqKey="Howard J" first="Jayda" last="Howard">Jayda Howard</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Molecular Diagnostic Laboratory, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Graham, Lisa" sort="Graham, Lisa" uniqKey="Graham L" first="Lisa" last="Graham">Lisa Graham</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Molecular Diagnostic Laboratory, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Chernos, Judy" sort="Chernos, Judy" uniqKey="Chernos J" first="Judy" last="Chernos">Judy Chernos</name>
<affiliation wicri:level="4"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Medical Genetics, University of Calgary, Calgary</wicri:regionArea>
<orgName type="university">Université de Calgary</orgName>
<placeName><settlement type="city">Calgary</settlement>
<region type="state">Alberta</region>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Cytogenetics Laboratory, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Bridge, Peter J" sort="Bridge, Peter J" uniqKey="Bridge P" first="Peter J." last="Bridge">Peter J. Bridge</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Molecular Diagnostic Laboratory, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
<affiliation wicri:level="4"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Medical Genetics, University of Calgary, Calgary</wicri:regionArea>
<orgName type="university">Université de Calgary</orgName>
<placeName><settlement type="city">Calgary</settlement>
<region type="state">Alberta</region>
</placeName>
</affiliation>
<affiliation wicri:level="4"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Pathology and Laboratory Medicine, University of Calgary, Calgary</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="Parboosingh, Jillian S" sort="Parboosingh, Jillian S" uniqKey="Parboosingh J" first="Jillian S." last="Parboosingh">Jillian S. Parboosingh</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Molecular Diagnostic Laboratory, Alberta Children's Hospital, Calgary</wicri:regionArea>
<wicri:noRegion>Calgary</wicri:noRegion>
</affiliation>
<affiliation wicri:level="4"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Medical Genetics, University of Calgary, Calgary</wicri:regionArea>
<orgName type="university">Université de Calgary</orgName>
<placeName><settlement type="city">Calgary</settlement>
<region type="state">Alberta</region>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country>Canada</country>
<wicri:regionArea>Molecular Diagnostic Laboratory, Alberta Children's Hospital, 2888 Shaganappi Trail NW, Calgary, Alberta</wicri:regionArea>
<wicri:noRegion>Alberta</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j" type="main">American Journal of Medical Genetics Part A</title>
<title level="j" type="alt">AMERICAN JOURNAL OF MEDICAL GENETICS</title>
<idno type="ISSN">1552-4825</idno>
<idno type="eISSN">1552-4833</idno>
<imprint><biblScope unit="vol">146A</biblScope>
<biblScope unit="issue">8</biblScope>
<biblScope unit="page" from="1067">1067</biblScope>
<biblScope unit="page" to="1071">1071</biblScope>
<biblScope unit="page-count">5</biblScope>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2008-04-15">2008-04-15</date>
</imprint>
<idno type="ISSN">1552-4825</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">1552-4825</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 007032 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 007032 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= Main |étape= Merge |type= RBID |clé= ISTEX:A6AE0FA77B39EB44407CAAC30CB96A9E85714668 |texte= An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier }}
![]() | This area was generated with Dilib version V0.6.31. | ![]() |