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...

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Detalles Bibliográficos
Autores principales: Zarate, Yuri A., Fish, Jennifer L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Research Reviews
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

Internet

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

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