A carregar...
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management
BACKGROUND: Rubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, with an estimated prevalence of one case per 125,000 live births. RSTS is characterized by typical facial features, microcephaly, broad thumbs and first toes, intellectual disability, and postnatal...
Na minha lista:
| Publicado no: | Ital J Pediatr |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4308897/ https://ncbi.nlm.nih.gov/pubmed/25599811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-015-0110-1 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|