Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome

dc.contributorGreenwood Genetic Center
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade do Estado do Rio de Janeiro (UERJ)
dc.contributorClemson University
dc.date.accessioned2014-05-27T11:25:51Z
dc.date.accessioned2022-10-05T18:26:34Z
dc.date.available2014-05-27T11:25:51Z
dc.date.available2022-10-05T18:26:34Z
dc.date.created2014-05-27T11:25:51Z
dc.date.issued2011-05-01
dc.identifierAmerican Journal of Medical Genetics, Part A, v. 155, n. 5, p. 988-992, 2011.
dc.identifier1552-4825
dc.identifier1552-4833
dc.identifierhttp://hdl.handle.net/11449/72395
dc.identifier10.1002/ajmg.a.33960
dc.identifier2-s2.0-79954998470
dc.identifier0000-0002-9256-7623
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3921461
dc.languageeng
dc.relationAmerican Journal of Medical Genetics Part A
dc.relation2.264
dc.relation1,098
dc.relation1,098
dc.rightsAcesso aberto
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 syndrome
dc.typeCarta


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