<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(8)</volume><submitter>Bergmann C</submitter><journal>European journal of human genetics : EJHG</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4970697</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical utility gene card for: Meckel syndrome - update 2016.</pubmed_title><pmcid>PMC4970697</pmcid><pubmed_authors>Salonen R</pubmed_authors><pubmed_authors>Bergmann C</pubmed_authors><pubmed_authors>Frank V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical utility gene card for: Meckel syndrome - update 2016.</name><description/><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Aug</publication><modification>2025-04-26T22:06:35.043Z</modification><creation>2025-04-06T17:00:45.959Z</creation></dates><accession>S-EPMC4970697</accession><cross_references><pubmed>27094752</pubmed><doi>10.1038/ejhg.2016.33</doi></cross_references></HashMap>