You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/72395
Full metadata record
DC FieldValueLanguage
dc.contributor.authorVieira, Gustavo H.-
dc.contributor.authorRodriguez, Jayson D.-
dc.contributor.authorBoy, Raquel-
dc.contributor.authorPaiva, Isaias Soares de-
dc.contributor.authorDupont, Barbara R.-
dc.contributor.authorMoretti-Ferreira, Danilo-
dc.contributor.authorSrivastava, Anand K.-
dc.date.accessioned2014-05-27T11:25:51Z-
dc.date.accessioned2016-10-25T18:33:50Z-
dc.date.available2014-05-27T11:25:51Z-
dc.date.available2016-10-25T18:33:50Z-
dc.date.issued2011-05-01-
dc.identifierhttp://dx.doi.org/10.1002/ajmg.a.33960-
dc.identifier.citationAmerican Journal of Medical Genetics, Part A, v. 155, n. 5, p. 988-992, 2011.-
dc.identifier.issn1552-4825-
dc.identifier.issn1552-4833-
dc.identifier.urihttp://hdl.handle.net/11449/72395-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/72395-
dc.format.extent988-992-
dc.language.isoeng-
dc.sourceScopus-
dc.subject1p36 deletion syndrome-
dc.subjectadolescent-
dc.subjectbehavior disorder-
dc.subjectcase report-
dc.subjectchromosome deletion-
dc.subjectclinical feature-
dc.subjectcomparative genomic hybridization-
dc.subjectcraniofacial malformation-
dc.subjectdifferential diagnosis-
dc.subjectfemale-
dc.subjectgenotype-
dc.subjecthuman-
dc.subjectintellectual impairment-
dc.subjectletter-
dc.subjectmuscle hypotonia-
dc.subjectpriority journal-
dc.subjectseizure-
dc.subjectsingle nucleotide polymorphism-
dc.subjectsleep disorder-
dc.subjectSmith Magenis syndrome-
dc.subjectspeech disorder-
dc.subjectAdolescent-
dc.subjectChromosome Deletion-
dc.subjectChromosomes, Human, Pair 1-
dc.subjectDiagnosis, Differential-
dc.subjectFemale-
dc.subjectHumans-
dc.subjectSmith-Magenis Syndrome-
dc.subjectSyndrome-
dc.titleDifferential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndromeen
dc.typeoutro-
dc.contributor.institutionGreenwood Genetic Center-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade do Estado do Rio de Janeiro (UERJ)-
dc.contributor.institutionClemson University-
dc.description.affiliationJ.C. Self Research Institute of Human Genetics Greenwood Genetic Center, Greenwood, SC-
dc.description.affiliationDepartment of Genetics University of São Paulo State, Botucatu, SP-
dc.description.affiliationFaculty of Medical Sciences Department of Pediatrics State University of Rio de Janeiro, Rio de Janeiro-
dc.description.affiliationDepartment of Genetics and Biochemistry Clemson University, Clemson, SC-
dc.identifier.doi10.1002/ajmg.a.33960-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
dc.identifier.scopus2-s2.0-79954998470-
dc.identifier.orcid0000-0002-9256-7623pt
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.