Cargando…
MYT1 role in the microtia‐craniofacial microsomia spectrum
BACKGROUND: Craniofacial microsomia (CFM), also known as the oculo‐auriculo‐vertebral spectrum, comprises a variable phenotype with the most common features including microtia and mandibular hypoplasia on one or both sides, in addition to lateral oral clefts, epibulbar dermoids, cardiac, vertebral,...
Autores principales: | Luquetti, Daniela V., Heike, Carrie L., Zarante, Ignacio, Timms, Andrew E., Gustafson, Jonas, Pachajoa, Harry, Porras‐Hurtado, Gloria L., Ayala‐Ramirez, Paola, Duenas‐Roque, Milagros M., Jimenez, Natalia, Ibanez, Lina M., Hurtado‐Villa, Paula |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549594/ https://www.ncbi.nlm.nih.gov/pubmed/32871052 http://dx.doi.org/10.1002/mgg3.1401 |
Ejemplares similares
-
Damaging variants in FOXI3 cause microtia and craniofacial microsomia
por: Quiat, Daniel, et al.
Publicado: (2023) -
1. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia
por: Timberlake, Andrew T., et al.
Publicado: (2023) -
PC16. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia
por: Timberlake, Andrew T., et al.
Publicado: (2023) -
Haploinsufficiency of SF3B2 causes craniofacial microsomia
por: Timberlake, Andrew T., et al.
Publicado: (2021) -
Reliable classification of facial phenotypic variation in craniofacial microsomia: a comparison of physical exam and photographs
por: Birgfeld, Craig B., et al.
Publicado: (2016)