DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism
| Autor: | Chen, Yunjia, Karaca, Ender, Robin, Nathaniel H., Goodloe, Dana, Al-Beshri, Ali, Dean, S. Joy, Hurst, Anna C.E., Carroll, Andrew J., Mikhail, Fady M. |
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| Zdroj: | In Genetics in Medicine January 2024 26(1) |
| Databáze: | ScienceDirect |
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