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Genes, crianças e pediatras: Neurofibromatose tipo 1

dc.contributor.authorBarbosa, M.
dc.contributor.authorPinto-Basto, J.
dc.contributor.authorLima, M.
dc.contributor.authorFortuna, A.
dc.contributor.authorSoares, G.
dc.date.accessioned2012-07-31T12:18:23Z
dc.date.available2012-07-31T12:18:23Z
dc.date.issued2009-06
dc.description.abstractCriança do sexo masculino avaliada pela primeira vez na consulta de Genética aos 4 anos e 4 meses, com de manchas café com leite, efélides axilares e inguinais, convulsões e compromisso do desenvolvimento psicomotor. A mãe do doente apresenta QI borderline, manchas café com leite, neurofi bromas, axilar e inguinal, nódulos de Lisch e glioma do nervo óptico.por
dc.identifier.citationNascer e Crescer 2009; 18(2): 130-132por
dc.identifier.issn0872-0754
dc.identifier.urihttp://hdl.handle.net/10400.16/1250
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherNascer e Crescerpor
dc.titleGenes, crianças e pediatras: Neurofibromatose tipo 1por
dc.title.alternativeGenes, children and paediatricians: Neurofibromatosis type 1por
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.endPage132por
oaire.citation.issue18(2)por
oaire.citation.startPage130por
oaire.citation.titleNascer e Crescerpor
oaire.citation.volume18por
person.familyNameFortuna
person.givenNameAna
person.identifier.orcid0000-0002-1296-5366
person.identifier.scopus-author-id35974338400
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicationb65d1d1e-7f2c-4f84-8189-2c37e7a2632f
relation.isAuthorOfPublication.latestForDiscoveryb65d1d1e-7f2c-4f84-8189-2c37e7a2632f

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