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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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Библиографические подробности
Опубликовано в: :PLoS One
Главные авторы: Gilbert, James R., Losee, Joseph E., Mooney, Mark P., Cray, James J., Gustafson, Jennifer, Cunningham, Michael L., Cooper, Gregory M.
Формат: Artigo
Язык:Inglês
Опубликовано: Public Library of Science 2018
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Online-ссылка: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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