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<meta name="keywords" content="C4016425, finding, gilbert syndrome, susceptibility to, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="" /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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||
UID=864862
|
||
ConceptID=C4016425
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Gilbert syndrome, susceptibility to</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>864862</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C4016425</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>GILBERT SYNDROME, SUSCEPTIBILITY TO</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>OMIM<span class="superscript">®</span>:</td>
|
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<td><a href="https://omim.org/entry/191740" target="_blank">191740</a></td></tr>
|
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</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_105">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/27664246">Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Paluch-Shimon S,
|
||
Cardoso F,
|
||
Sessa C,
|
||
Balmana J,
|
||
Cardoso MJ,
|
||
Gilbert F,
|
||
Senkus E;
|
||
ESMO Guidelines Committee</span><br />
|
||
<span class="medgenPMjournal">Ann Oncol</span>
|
||
2016 Sep;27(suppl 5):v103-v110.
|
||
doi: 10.1093/annonc/mdw327.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27664246" target="_blank">27664246</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25299866">Detection and management of drug-resistant tuberculosis in HIV-infected patients in lower-income countries.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ballif M,
|
||
Nhandu V,
|
||
Wood R,
|
||
Dusingize JC,
|
||
Carter EJ,
|
||
Cortes CP,
|
||
McGowan CC,
|
||
Diero L,
|
||
Graber C,
|
||
Renner L,
|
||
Hawerlander D,
|
||
Kiertiburanakul S,
|
||
Du QT,
|
||
Sterling TR,
|
||
Egger M,
|
||
Fenner L;
|
||
International epidemiological Databases to Evaluate AIDS (IeDEA)</span><br />
|
||
<span class="medgenPMjournal">Int J Tuberc Lung Dis</span>
|
||
2014 Nov;18(11):1327-36.
|
||
doi: 10.5588/ijtld.14.0106.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25299866" target="_blank">25299866</a><a href="/pmc/articles/PMC4323497" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24687378">MRI breast screening in high-risk women: cancer detection and survival analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Evans DG,
|
||
Kesavan N,
|
||
Lim Y,
|
||
Gadde S,
|
||
Hurley E,
|
||
Massat NJ,
|
||
Maxwell AJ,
|
||
Ingham S,
|
||
Eeles R,
|
||
Leach MO;
|
||
MARIBS Group,
|
||
Howell A,
|
||
Duffy SW</span><br />
|
||
<span class="medgenPMjournal">Breast Cancer Res Treat</span>
|
||
2014 Jun;145(3):663-72.
|
||
Epub 2014 Apr 1
|
||
doi: 10.1007/s10549-014-2931-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24687378" target="_blank">24687378</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(gilbert%20syndrome%2C%20susceptibility%20to)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (23)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34237774">Mapping the human genetic architecture of COVID-19.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">COVID-19 Host Genetics Initiative</span><br />
|
||
<span class="medgenPMjournal">Nature</span>
|
||
2021 Dec;600(7889):472-477.
|
||
Epub 2021 Jul 8
|
||
doi: 10.1038/s41586-021-03767-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34237774" target="_blank">34237774</a><a href="/pmc/articles/PMC8674144" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31835028">Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cross-Disorder Group of the Psychiatric Genomics Consortium. Electronic address: plee0@mgh.harvard.edu;
|
||
Cross-Disorder Group of the Psychiatric Genomics Consortium</span><br />
|
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<span class="medgenPMjournal">Cell</span>
|
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2019 Dec 12;179(7):1469-1482.e11.
|
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doi: 10.1016/j.cell.2019.11.020.
|
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<span class="bold">PMID: </span><a href="/pubmed/31835028" target="_blank">31835028</a><a href="/pmc/articles/PMC7077032" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
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<div class="nl"><a target="_blank" href="/pubmed/30820047">Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Kunkle BW,
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<span class="medgenPMjournal">Nat Genet</span>
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2019 Mar;51(3):414-430.
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Epub 2019 Feb 28
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doi: 10.1038/s41588-019-0358-2.
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<span class="bold">PMID: </span><a href="/pubmed/30820047" target="_blank">30820047</a><a href="/pmc/articles/PMC6463297" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
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<div class="nl"><a target="_blank" href="/pubmed/28714976">Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Sims R,
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van der Lee SJ,
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Naj AC,
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|
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<div class="nl"><a target="_blank" href="/pubmed/17554300">Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.</a></div>
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|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Gilbert%20syndrome%2C%20susceptibility%20to%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (150)</a></div></div>
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</div>
|
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|
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<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln">
|
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<div class="nl"><a target="_blank" href="/pubmed/36940245">Single Nucleotide Polymorphisms and Adolescent Idiopathic Scoliosis: A Systematic Review and Meta-Analysis of the Literature.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">AlMekkawi AK,
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Caruso JP,
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El Ahmadieh TY,
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Palmisciano P,
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Aljardali MW,
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Derian AG,
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Al Tamimi M,
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Bagley CA,
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Aoun SG</span><br />
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<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
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2023 May 15;48(10):695-701.
|
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Epub 2023 Mar 13
|
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doi: 10.1097/BRS.0000000000004623.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36940245" target="_blank">36940245</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/36894397">Uptake of Mpox vaccination among transgender people and gay, bisexual and other men who have sex with men among sexually-transmitted infection clinic clients in Vancouver, British Columbia.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Gilbert M,
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Ablona A,
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Chang HJ,
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Grennan T,
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Irvine MA,
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Sarai Racey C,
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<span class="medgenPMjournal">Vaccine</span>
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2023 Apr 6;41(15):2485-2494.
|
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Epub 2023 Mar 7
|
||
doi: 10.1016/j.vaccine.2023.02.075.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36894397" target="_blank">36894397</a><a href="/pmc/articles/PMC9990897" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34904276">Foetal alcohol spectrum disorder and Investigative interviewing: A systematic review highlighting clinical and legal implications and recommendations.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Gilbert DJ,
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Allely CS,
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||
Mukherjee RAS,
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||
Cook PA</span><br />
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<span class="medgenPMjournal">Behav Sci Law</span>
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Epub 2021 Dec 13
|
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doi: 10.1002/bsl.2552.
|
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<span class="bold">PMID: </span><a href="/pubmed/34904276" target="_blank">34904276</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Gilbert%20syndrome%2C%20susceptibility%20to%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (3)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
||
<div class="portlet mgSection" id="ID_113">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul id="my-toc"></ul></div>
|
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</div>
|
||
|
||
<div class="portlet mgSection" id="ID_106">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C4016425%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (10)</a></li>
|
||
<li><a href="/gtr/tests?term=C4016425%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (14)</a></li>
|
||
<li><a href="/gtr/tests?term=C4016425%5bDISCUI%5d&filter=method%3A2%5F19" target="_blank">Targeted variant analysis (1)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C4016425%5bDISCUI%5d" target="_blank">See all (16)</a></total></li>
|
||
</ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_119">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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