Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex

The phenotype currently accepted as Pierre Robin syndrome/sequence/anomalad/complex (PR) is characterized by mandibular dysmorphology, glossoptosis, respiratory obstruction, and in some cases, cleft palate. A causative sequence of developmental events is hypothesized for PR, but few clear causal rel...

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Detalles Bibliográficos
Autores principales: Motch Perrine, Susan M., Wu, Meng, Holmes, Greg, Bjork, Bryan C., Jabs, Ethylin Wang, Richtsmeier, Joan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768358/
https://www.ncbi.nlm.nih.gov/pubmed/33291480
http://dx.doi.org/10.3390/jdb8040030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768358/
https://www.ncbi.nlm.nih.gov/pubmed/33291480
http://dx.doi.org/10.3390/jdb8040030

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