Cite
HARVARD Citation
Gaspar, H. et al. (2017). 4.7 Mb deletion encompassing TGFB2 associated with features of Loeys–Dietz syndrome and osteoporosis in adulthood. American journal of medical genetics. 173 (8), pp. 2289-2292. [Online].
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Gaspar, H. et al. (2017). 4.7 Mb deletion encompassing TGFB2 associated with features of Loeys–Dietz syndrome and osteoporosis in adulthood. American journal of medical genetics. 173 (8), pp. 2289-2292. [Online].