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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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| 出版年: | PLoS One |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2018
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| 主題: | |
| オンライン･アクセス: | 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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