<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(1)</volume><submitter>Martin S</submitter><journal>Orphanet journal of rare diseases</journal><pagination>27</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12836846</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022.</pubmed_title><pmcid>PMC12836846</pmcid><pubmed_authors>Martinez-Fresno M</pubmed_authors><pubmed_authors>Gross ES</pubmed_authors><pubmed_authors>Audi J</pubmed_authors><pubmed_authors>Grauman A</pubmed_authors><pubmed_authors>Raming R</pubmed_authors><pubmed_authors>Velinov B</pubmed_authors><pubmed_authors>Zak M</pubmed_authors><pubmed_authors>Agolini E</pubmed_authors><pubmed_authors>Courbier S</pubmed_authors><pubmed_authors>Kyosovska-Peshtenska G</pubmed_authors><pubmed_authors>Knieling F</pubmed_authors><pubmed_authors>Man Y</pubmed_authors><pubmed_authors>Piperkova A</pubmed_authors><pubmed_authors>Wagner A</pubmed_authors><pubmed_authors>Gumus G</pubmed_authors><pubmed_authors>Martin S</pubmed_authors><pubmed_authors>Kirschner J</pubmed_authors><pubmed_authors>Furer A</pubmed_authors><pubmed_authors>Fortunato F</pubmed_authors><pubmed_authors>Bruno LP</pubmed_authors><pubmed_authors>Novelli A</pubmed_authors><pubmed_authors>Jackson T</pubmed_authors><pubmed_authors>Hansson M</pubmed_authors><pubmed_authors>Veldwijk J</pubmed_authors><pubmed_authors>Saier C</pubmed_authors><pubmed_authors>Frankova V</pubmed_authors><pubmed_authors>Coulter J</pubmed_authors><pubmed_authors>Ottombrino S</pubmed_authors><pubmed_authors>Zarakowska K</pubmed_authors><pubmed_authors>Garnier N</pubmed_authors><pubmed_authors>Granados A</pubmed_authors><pubmed_authors>Sansen S</pubmed_authors><pubmed_authors>Hauber B</pubmed_authors><pubmed_authors>Dubief J</pubmed_authors><pubmed_authors>Bertini ES</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022.</name><description/><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-16T03:08:57.578Z</modification><creation>2026-06-16T03:06:48.058Z</creation></dates><accession>S-EPMC12836846</accession><cross_references><pubmed>41507926</pubmed><doi>10.1186/s13023-025-04179-0</doi></cross_references></HashMap>