Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype
| Autor: | Deanna Fry, Daniel Groepper, Gretchen MacCarrick, Erin M. Demo, Matthew J. Thomas, Margaret J. Wilkes, Michael J. Lyons, Megan E. Tucker, Catherine Steding, Julie Fleischer |
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| Rok vydání: | 2022 |
| Předmět: | |
| Zdroj: | American Journal of Medical Genetics Part A. 188:2237-2241 |
| ISSN: | 1552-4833 1552-4825 |
| Databáze: | OpenAIRE |
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