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http://acervodigital.unesp.br/handle/11449/72395
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Vieira, Gustavo H. | - |
dc.contributor.author | Rodriguez, Jayson D. | - |
dc.contributor.author | Boy, Raquel | - |
dc.contributor.author | Paiva, Isaias Soares de | - |
dc.contributor.author | Dupont, Barbara R. | - |
dc.contributor.author | Moretti-Ferreira, Danilo | - |
dc.contributor.author | Srivastava, Anand K. | - |
dc.date.accessioned | 2014-05-27T11:25:51Z | - |
dc.date.accessioned | 2016-10-25T18:33:50Z | - |
dc.date.available | 2014-05-27T11:25:51Z | - |
dc.date.available | 2016-10-25T18:33:50Z | - |
dc.date.issued | 2011-05-01 | - |
dc.identifier | http://dx.doi.org/10.1002/ajmg.a.33960 | - |
dc.identifier.citation | American Journal of Medical Genetics, Part A, v. 155, n. 5, p. 988-992, 2011. | - |
dc.identifier.issn | 1552-4825 | - |
dc.identifier.issn | 1552-4833 | - |
dc.identifier.uri | http://hdl.handle.net/11449/72395 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/72395 | - |
dc.format.extent | 988-992 | - |
dc.language.iso | eng | - |
dc.source | Scopus | - |
dc.subject | 1p36 deletion syndrome | - |
dc.subject | adolescent | - |
dc.subject | behavior disorder | - |
dc.subject | case report | - |
dc.subject | chromosome deletion | - |
dc.subject | clinical feature | - |
dc.subject | comparative genomic hybridization | - |
dc.subject | craniofacial malformation | - |
dc.subject | differential diagnosis | - |
dc.subject | female | - |
dc.subject | genotype | - |
dc.subject | human | - |
dc.subject | intellectual impairment | - |
dc.subject | letter | - |
dc.subject | muscle hypotonia | - |
dc.subject | priority journal | - |
dc.subject | seizure | - |
dc.subject | single nucleotide polymorphism | - |
dc.subject | sleep disorder | - |
dc.subject | Smith Magenis syndrome | - |
dc.subject | speech disorder | - |
dc.subject | Adolescent | - |
dc.subject | Chromosome Deletion | - |
dc.subject | Chromosomes, Human, Pair 1 | - |
dc.subject | Diagnosis, Differential | - |
dc.subject | Female | - |
dc.subject | Humans | - |
dc.subject | Smith-Magenis Syndrome | - |
dc.subject | Syndrome | - |
dc.title | Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome | en |
dc.type | outro | - |
dc.contributor.institution | Greenwood Genetic Center | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.contributor.institution | Universidade do Estado do Rio de Janeiro (UERJ) | - |
dc.contributor.institution | Clemson University | - |
dc.description.affiliation | J.C. Self Research Institute of Human Genetics Greenwood Genetic Center, Greenwood, SC | - |
dc.description.affiliation | Department of Genetics University of São Paulo State, Botucatu, SP | - |
dc.description.affiliation | Faculty of Medical Sciences Department of Pediatrics State University of Rio de Janeiro, Rio de Janeiro | - |
dc.description.affiliation | Department of Genetics and Biochemistry Clemson University, Clemson, SC | - |
dc.identifier.doi | 10.1002/ajmg.a.33960 | - |
dc.rights.accessRights | Acesso restrito | - |
dc.relation.ispartof | American Journal of Medical Genetics Part A | - |
dc.identifier.scopus | 2-s2.0-79954998470 | - |
dc.identifier.orcid | 0000-0002-9256-7623 | pt |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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