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Caso hematológico: Anemia de Fanconi

dc.contributor.authorNascimento, P.
dc.contributor.authorCosta, E.
dc.contributor.authorPorto, B.
dc.contributor.authorBarbot, J.
dc.date.accessioned2012-06-26T10:03:51Z
dc.date.available2012-06-26T10:03:51Z
dc.date.issued2010-09
dc.description.abstractThe authors present the case of a child with complex congenital heart defect, bilateral malformation of the thumbs, hearing loss, failure to thrive and delayed psychomotor development, oriented to the hematology consultation at the age of 9 years for the presence of thrombocytopenia and macrocytosis.por
dc.identifier.citationNascer e Crescer 2010; 19(3): 166-168por
dc.identifier.issn0872-0754
dc.identifier.urihttp://hdl.handle.net/10400.16/1061
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherNascer e Crescerpor
dc.subjectAnemia de Fanconipor
dc.subjectFanconi anemiapor
dc.titleCaso hematológico: Anemia de Fanconipor
dc.title.alternativeHematologic case: Fanconi anemiapor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.endPage168por
oaire.citation.issue19(3)por
oaire.citation.startPage166por
oaire.citation.titleNascer e Crescerpor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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