PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome
| Autor: | Abdin, D., Rump, A., Tzschach, A., Sarnow, K., Schröck, E., Hackmann, K., Di Donato, N. |
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| Zdroj: | In European Journal of Medical Genetics December 2019 62(12) |
| Databáze: | ScienceDirect |
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