Cargando…
SATB2‐associated syndrome: Mechanisms, phenotype, and practical recommendations
The SATB2‐associated syndrome is a recently described syndrome characterized by developmental delay/intellectual disability with absent or limited speech development, craniofacial abnormalities, behavioral problems, dysmorphic features, and palatal and dental abnormalities. Alterations of the SATB2...
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2016
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297989/ https://www.ncbi.nlm.nih.gov/pubmed/27774744 http://dx.doi.org/10.1002/ajmg.a.38022 |