Baena, N., Monk, D., Aguilera, C., Fraga, M. F., Fernández, A. F., Gabau, E., . . . Guitart, M. (2024). Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome.
Citación estilo ChicagoBaena, Neus, et al. Novel 14q32.2 Paternal Deletion Encompassing the Whole DLK1 Gene Associated With Temple Syndrome. 2024.
Cita MLABaena, Neus, et al. Novel 14q32.2 Paternal Deletion Encompassing the Whole DLK1 Gene Associated With Temple Syndrome. 2024.
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