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Predicting Modifiers of Genotype-Phenotype Correlations in Craniofacial Development

Most human birth defects are phenotypically variable even when they share a common genetic basis. Our understanding of the mechanisms of this variation is limited, but they are thought to be due to complex gene-environment interactions. Loss of the transcription factor Gata3 associates with the high...

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Detalles Bibliográficos
Autores principales: Kar, Ranjeet D., Eberhart, Johann K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864425/
https://www.ncbi.nlm.nih.gov/pubmed/36674738
http://dx.doi.org/10.3390/ijms24021222

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