Cite
HARVARD Citation
Fry, D. et al. (2022). Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype. American journal of medical genetics. 188 (7), pp. 2237-2241. [Online].
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Fry, D. et al. (2022). Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype. American journal of medical genetics. 188 (7), pp. 2237-2241. [Online].