<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(4)</volume><submitter>Tien DA</submitter><pubmed_abstract>We report a rare case of tetralogy of Fallot with dextrocardia and anomalous coronary artery. Although this is an unusual complex disease, we have successfully repaired it with a combination of transatrial/transpulmonary and trans-right ventricle techniques.</pubmed_abstract><journal>World journal for pediatric &amp; congenital heart surgery</journal><pagination>522-524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7343333</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tetralogy of Fallot With Dextrocardia and Anomalous Coronary Artery: A Case Report.</pubmed_title><pmcid>PMC7343333</pmcid><pubmed_authors>Nguyen TT</pubmed_authors><pubmed_authors>Tien DA</pubmed_authors><pubmed_authors>Thanh LN</pubmed_authors><pubmed_authors>Linh NTH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tetralogy of Fallot With Dextrocardia and Anomalous Coronary Artery: A Case Report.</name><description>We report a rare case of tetralogy of Fallot with dextrocardia and anomalous coronary artery. Although this is an unusual complex disease, we have successfully repaired it with a combination of transatrial/transpulmonary and trans-right ventricle techniques.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-05T15:21:18.803Z</modification><creation>2025-04-05T15:21:18.803Z</creation></dates><accession>S-EPMC7343333</accession><cross_references><pubmed>32195621</pubmed><doi>10.1177/2150135120911342</doi></cross_references></HashMap>