V. Agostini Et Al. , "Biallelic truncating variants in VGLL2 cause syngnathia in humans," Journal of Medical Genetics , vol.60, no.11, pp.1084-1091, 2023
Agostini, V. Et Al. 2023. Biallelic truncating variants in VGLL2 cause syngnathia in humans. Journal of Medical Genetics , vol.60, no.11 , 1084-1091.
Agostini, V., Tessier, A., Djaziri, N., Khonsari, R. H., Galliani, E., Kurihara, Y., ... Honda, M.(2023). Biallelic truncating variants in VGLL2 cause syngnathia in humans. Journal of Medical Genetics , vol.60, no.11, 1084-1091.
Agostini, Valeria Et Al. "Biallelic truncating variants in VGLL2 cause syngnathia in humans," Journal of Medical Genetics , vol.60, no.11, 1084-1091, 2023
Agostini, Valeria Et Al. "Biallelic truncating variants in VGLL2 cause syngnathia in humans." Journal of Medical Genetics , vol.60, no.11, pp.1084-1091, 2023
Agostini, V. Et Al. (2023) . "Biallelic truncating variants in VGLL2 cause syngnathia in humans." Journal of Medical Genetics , vol.60, no.11, pp.1084-1091.
@article{article, author={Valeria Agostini Et Al. }, title={Biallelic truncating variants in VGLL2 cause syngnathia in humans}, journal={Journal of Medical Genetics}, year=2023, pages={1084-1091} }