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Prenatal screening and diagnosis of genetic abnormalities: sego, seqcml, aedp consensus recommendations

dc.contributor.authorPrieto García, Belén 
dc.contributor.authorAdiego, B.
dc.contributor.authorSuela, J.
dc.contributor.authorMartín, I.
dc.contributor.authorSantacruz, B.
dc.contributor.authorGarcía Planells, J.
dc.contributor.authorGil, M.
dc.contributor.authorGonzález, C.
dc.contributor.authorBarrenechea, E.
dc.date.accessioned2023-02-01T11:50:27Z
dc.date.available2023-02-01T11:50:27Z
dc.date.issued2020
dc.identifier.citationAdvances in Laboratory Medicine, 1(3) (2020); doi:10.1515/almed-2020-0043
dc.identifier.issn2628-491X
dc.identifier.urihttp://hdl.handle.net/10651/65922
dc.language.isoeng
dc.relation.ispartofAdvances in Laboratory Medicine
dc.rights© 2020 Belén Prieto et al., published by De Gruyter.
dc.rightsCC Reconocimiento 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85129734986&doi=10.1515%2falmed-2020-0043&partnerID=40&md5=b2ff39066c655da7279a32e20a79c8f3
dc.titlePrenatal screening and diagnosis of genetic abnormalities: sego, seqcml, aedp consensus recommendations
dc.typejournal article
dc.identifier.doi10.1515/almed-2020-0043
dc.relation.publisherversionhttp://dx.doi.org/10.1515/almed-2020-0043
dc.rights.accessRightsopen access
dc.type.hasVersionVoR


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© 2020 Belén Prieto et al., published by De Gruyter.
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