Cargando…
Abstract QS43: Blepharophimosis Ptosis Epicanthus Inversus Syndrome Caused by a ZC3H13 Gene Mutation
Autores principales: | Balkin, Daniel M., Nelson-Williams, Carol, Sumpio, Brandon J., Scott, Daryl A., Pabic, Pierre Le, Schilling, Thomas F., Lifton, Richard P., Narayan, Deepak |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959671/ http://dx.doi.org/10.1097/01.GOX.0000534051.38103.88 |
Ejemplares similares
-
A rare cause of congenital ptosis: Blepharophimosis, ptosis and epicanthus inversus syndrome
por: Setty, Gururaj, et al.
Publicado: (2012) -
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome
por: Wang, Juan, et al.
Publicado: (2007) -
Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family
por: Gupta, Abhinav Kumar, et al.
Publicado: (2017) -
Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome: A Simple Remedy for Challenging Cases
por: Alkhairy, Saba, et al.
Publicado: (2022) -
The Genetic and Clinical Features of FOXL2-Related Blepharophimosis, Ptosis and Epicanthus Inversus Syndrome
por: Méjécase, Cécile, et al.
Publicado: (2021)