dc.contributor | Greenwood Genetic Center | |
dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.contributor | Universidade do Estado do Rio de Janeiro (UERJ) | |
dc.contributor | Clemson University | |
dc.date.accessioned | 2014-05-27T11:25:51Z | |
dc.date.accessioned | 2022-10-05T18:26:34Z | |
dc.date.available | 2014-05-27T11:25:51Z | |
dc.date.available | 2022-10-05T18:26:34Z | |
dc.date.created | 2014-05-27T11:25:51Z | |
dc.date.issued | 2011-05-01 | |
dc.identifier | American Journal of Medical Genetics, Part A, v. 155, n. 5, p. 988-992, 2011. | |
dc.identifier | 1552-4825 | |
dc.identifier | 1552-4833 | |
dc.identifier | http://hdl.handle.net/11449/72395 | |
dc.identifier | 10.1002/ajmg.a.33960 | |
dc.identifier | 2-s2.0-79954998470 | |
dc.identifier | 0000-0002-9256-7623 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/3921461 | |
dc.language | eng | |
dc.relation | American Journal of Medical Genetics Part A | |
dc.relation | 2.264 | |
dc.relation | 1,098 | |
dc.relation | 1,098 | |
dc.rights | Acesso aberto | |
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 | |
dc.type | Carta | |