Aberrant cell segregation in the craniofacial primordium and the emergence of facial dysmorphology in craniofrontonasal syndrome

Craniofrontonasal syndrome (CFNS) is a rare X-linked disorder characterized by craniofacial, skeletal, and neurological anomalies and is caused by mutations in EFNB1. Heterozygous females are more severely affected by CFNS than hemizygous males, a phenomenon called cellular interference that results...

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Detalles Bibliográficos
Autores principales: Niethamer, Terren K., Teng, Teng, Franco, Melanie, Du, Yu Xin, Percival, Christopher J., Bush, Jeffrey O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058351/
https://www.ncbi.nlm.nih.gov/pubmed/32092051
http://dx.doi.org/10.1371/journal.pgen.1008300

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058351/
https://www.ncbi.nlm.nih.gov/pubmed/32092051
http://dx.doi.org/10.1371/journal.pgen.1008300

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