Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome
| Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
|---|---|
| Data(s) |
27/05/2014
27/05/2014
01/05/2011
|
| Formato |
988-992 |
| Identificador |
http://dx.doi.org/10.1002/ajmg.a.33960 American Journal of Medical Genetics, Part A, v. 155, n. 5, p. 988-992, 2011. 1552-4825 1552-4833 http://hdl.handle.net/11449/72395 10.1002/ajmg.a.33960 2-s2.0-79954998470 |
| Idioma(s) |
eng |
| Relação |
American Journal of Medical Genetics Part A |
| Direitos |
closedAccess |
| Palavras-Chave | #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 |
| Tipo |
info:eu-repo/semantics/other |
