You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/72395
Title: 
Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome
Author(s): 
Institution: 
  • Greenwood Genetic Center
  • Universidade Estadual Paulista (UNESP)
  • Universidade do Estado do Rio de Janeiro (UERJ)
  • Clemson University
ISSN: 
  • 1552-4825
  • 1552-4833
Issue Date: 
1-May-2011
Citation: 
American Journal of Medical Genetics, Part A, v. 155, n. 5, p. 988-992, 2011.
Time Duration: 
988-992
Keywords: 
  • 1p36 deletion syndrome
  • adolescent
  • behavior disorder
  • case report
  • chromosome deletion
  • clinical feature
  • comparative genomic hybridization
  • craniofacial malformation
  • differential diagnosis
  • female
  • genotype
  • human
  • intellectual impairment
  • letter
  • muscle hypotonia
  • priority journal
  • seizure
  • single nucleotide polymorphism
  • sleep disorder
  • Smith Magenis syndrome
  • speech disorder
  • Adolescent
  • Chromosome Deletion
  • Chromosomes, Human, Pair 1
  • Diagnosis, Differential
  • Female
  • Humans
  • Smith-Magenis Syndrome
  • Syndrome
Source: 
http://dx.doi.org/10.1002/ajmg.a.33960
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/72395
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
Show full item record   View Statistics
 

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