Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/53280
DC FieldValueLanguage
dc.contributor.authorBeris, P
dc.contributor.authorMiescher, Pa
dc.contributor.authorDiazchico, Jc
dc.contributor.authorHan, Is
dc.contributor.authorKutlar, A
dc.contributor.authorHu, H
dc.contributor.authorWilson, Jb
dc.contributor.authorHuisman, Thj
dc.contributor.otherDiaz-Chico, Juan
dc.date.accessioned2019-02-04T15:57:14Z-
dc.date.available2019-02-04T15:57:14Z-
dc.date.issued1988
dc.identifier.issn0006-4971
dc.identifier.urihttp://hdl.handle.net/10553/53280-
dc.publisher0006-4971
dc.relation.ispartofBlood
dc.sourceBlood[ISSN 0006-4971],v. 72 (2), p. 801-805
dc.titleInclusion Body Beta-Thalassemia Trait In A Swiss Family Is Caused By An Abnormal Hemoglobin (Geneva) With An Altered And Extended-Beta Chain Carboxy-Terminus Due To A Modification In Codon Beta-114
dc.typeinfo:eu-repo/semantics/article
dc.typeArticle
dc.identifier.isiA1988P707200065
dcterms.isPartOfBlood
dcterms.sourceBlood[ISSN 0006-4971],v. 72 (2), p. 801-805
dc.description.lastpage805
dc.identifier.issue2
dc.description.firstpage801
dc.relation.volume72
dc.type2Artículo
dc.identifier.wosWOS:A1988P707200065
dc.contributor.daisngid28126659
dc.contributor.daisngid92733
dc.contributor.daisngid749099
dc.contributor.daisngid719735
dc.contributor.daisngid45319
dc.contributor.daisngid16328727
dc.contributor.daisngid91700
dc.contributor.daisngid4975
dc.identifier.investigatorRIDH-1527-2015
dc.identifier.ulpgces
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Bioquímica Farmacológica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología.-
crisitem.author.orcid0000-0002-0944-990X-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameDíaz Chico, Juan Carlos-
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