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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| 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 |