Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit

Craniosynostosis (CS) is a disorder that involves the premature ossification of one or more cranial sutures. Our research team has described a naturally occurring rabbit model of CS with a variable phenotype and unknown etiology. Restriction-site associated DNA (RAD) sequencing is a genomic sampling...

Descripción completa

Detalles Bibliográficos
Autores principales: Gilbert, James R., Losee, Joseph E., Mooney, Mark P., Cray, James J., Gustafson, Jennifer, Cunningham, Michael L., Cooper, Gregory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147457/
https://www.ncbi.nlm.nih.gov/pubmed/30235265
http://dx.doi.org/10.1371/journal.pone.0204086

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147457/
https://www.ncbi.nlm.nih.gov/pubmed/30235265
http://dx.doi.org/10.1371/journal.pone.0204086

Ejemplares similares