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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...
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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6147457/ https://ncbi.nlm.nih.gov/pubmed/30235265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0204086 |
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