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<div class="title"><a href="/gui2/?mode=browse¶ms=publication;21876669" target="_blank">Intragenic DNA Polymorphism Analysis of DMD/BMD Dystrophy Gene for Carrier and Prenatal Diagnosis in 60 Iranian Healthy Individuals</a></div> <div> <span class="journal-title">INTERNATIONAL JOURNAL OF NEUROSCIENCE</span>
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<pre class="comment" style="margin-top: 0; margin-bottom: 0;"><u>Megjegyzés</u>: WC: Neurosciences
Megjegyzés-22350237
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<div class="JournalArticle Publication short-list"> <div class="authors"> <span class="author-name" > Poulsen, L </span> <span class="author-type"> </span> ; <span class="author-name" > Horn, N </span> <span class="author-type"> </span> ; <span class="author-name" > Heilstrup, H </span> <span class="author-type"> </span> ; <span class="author-name" > Lund, C </span> <span class="author-type"> </span> ; <span class="author-name" > Tümer, Z </span> <span class="author-type"> </span> ; <span class="author-name" > Møller, L B </span> <span class="author-type"> </span> </div ><div class="title"><a href="/gui2/?mode=browse¶ms=publication;22350239" mtid="22350239" target="_blank">X-linked recessive Menkes disease: Identification of partial gene deletions in affected males</a></div> <div class="pub-info"> <span class="journal-title">CLINICAL GENETICS</span> <span class="journal-volume">62</span> : <span class="journal-issue">6</span> <span class="page"> pp. 449-457. , 9 p. </span> <span class="year">(2002)</span> </div> <div class="pub-end"><div class="identifier-list"> <span class="identifiers"> <span class="id identifier oa_none" title="none"> <a style="color:black" title="10.1034/j.1399-0004.2002.620605.x" target="_blank" href="https://doi.org/10.1034%2Fj.1399-0004.2002.620605.x"> DOI </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:black" title="000179771800007" target="_blank" href="http://gateway.isiknowledge.com/gateway/Gateway.cgi?&GWVersion=2&SrcAuth=CustomerName&SrcApp=CustomerName&DestLinkType=FullRecord&KeyUT=000179771800007&DestApp=WOS"> WoS </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:black" title="0036953710" target="_blank" href="http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-0036953710"> Scopus </a> </span> </span> </div> <span class="short-pub-prop-list"> <span class="short-pub-mtid"> Közlemény:22350239 </span> <span class="status-holder"><span class="status-data status-ADMIN_APPROVED"> Admin láttamozott </span></span> <span class="pub-core"> Idéző </span> <span class="pub-type">Folyóiratcikk </span> <!-- && !record.category.scientific --> </span> </div> </div><div class="JournalArticle Publication long-list">
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<div class="title"><a href="/gui2/?mode=browse¶ms=publication;22350239" target="_blank">X-linked recessive Menkes disease: Identification of partial gene deletions in affected males</a></div> <div> <span class="journal-title">CLINICAL GENETICS</span>
<span class="journal-issn">(<a target="_blank" href="https://portal.issn.org/resource/ISSN/0009-9163">0009-9163</a> <a target="_blank" href="https://portal.issn.org/resource/ISSN/1399-0004">1399-0004</a>)</span>:
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<pre class="comment" style="margin-top: 0; margin-bottom: 0;"><u>Megjegyzés</u>: Molecular Sequence Numbers: GENBANK: L06133, Z94801;
Chemicals/CAS: adenosine triphosphatase, 37289-25-1, 9000-83-3; amino acid, 65072-01-7; copper, 15158-11-9, 7440-50-8; Adenosine Triphosphatases, EC 3.6.1.-; ATP7A protein, human, EC 3.6.3.4; Cation Transport Proteins; DNA Primers; Recombinant Fusion Proteins</pre>
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<div class="JournalArticle Publication short-list"> <div class="authors"> <span class="author-name" > Chaturvedi, L S </span> <span class="author-type"> </span> ; <span class="author-name" > Srivastava, S </span> <span class="author-type"> </span> ; <span class="author-name" > Mukherjee, M </span> <span class="author-type"> </span> ; <span class="author-name" > Mittal, R D </span> <span class="author-type"> </span> ; <span class="author-name" > Phadke, S R </span> <span class="author-type"> </span> ; <span class="author-name" > Pradhan, S </span> <span class="author-type"> </span> ; <span class="author-name" > Mittal, B </span> <span class="author-type"> </span> </div ><div class="title"><a href="/gui2/?mode=browse¶ms=publication;22350240" mtid="22350240" target="_blank">Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene</a></div> <div class="pub-info"> <span class="journal-title">INDIAN JOURNAL OF MEDICAL RESEARCH</span> <span class="journal-volume">113</span> : <span class="journal-issue">JAN.</span> <span class="page"> pp. 19-25. , 7 p. </span> <span class="year">(2001)</span> </div> <div class="pub-end"><div class="identifier-list"> <span class="identifiers"> <span class="id identifier oa_none" title="none"> <a style="color:black" title="000167505900005" target="_blank" href="http://gateway.isiknowledge.com/gateway/Gateway.cgi?&GWVersion=2&SrcAuth=CustomerName&SrcApp=CustomerName&DestLinkType=FullRecord&KeyUT=000167505900005&DestApp=WOS"> WoS </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:black" title="0035075292" target="_blank" href="http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-0035075292"> Scopus </a> </span> </span> </div> <div class="short-pub-prop-list"> <span class="short-pub-mtid"> Közlemény:22350240 </span> <span class="status-holder"><span class="status-data status-ADMIN_APPROVED"> Admin láttamozott </span></span> <span class="pub-core"> Idéző </span> <span class="pub-type">Folyóiratcikk </span> <!-- && !record.category.scientific --> </div> </div> </div><div class="JournalArticle Publication long-list">
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<div class="title"><a href="/gui2/?mode=browse¶ms=publication;22350240" target="_blank">Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene</a></div> <div> <span class="journal-title">INDIAN JOURNAL OF MEDICAL RESEARCH</span>
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<pre class="comment" style="margin-top: 0; margin-bottom: 0;"><u>Megjegyzés</u>: Chemicals/CAS: Dystrophin</pre>
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