Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome

Facial dysmorphology is a hallmark of 22q11.2 deletion syndrome (22q11DS). Nearly all affected individuals have facial features characteristic of the syndrome: a vertically long face with broad nasal bridge, narrow palpebral fissures and mild micrognathia, sometimes accompanied by facial skeletal an...

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Detalles Bibliográficos
Autores principales: Paronett, Elizabeth M, Bryan, Corey A, Maynard, Megan E, Goroff, Julia A, Meechan, Daniel W, LaMantia, Anthony-Samuel, Maynard, Thomas M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244217/
https://www.ncbi.nlm.nih.gov/pubmed/36790128
http://dx.doi.org/10.1093/hmg/ddad030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244217/
https://www.ncbi.nlm.nih.gov/pubmed/36790128
http://dx.doi.org/10.1093/hmg/ddad030

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