Fadiga, L.; Lavrador, M.; Vicente, N.; Barros, L.; Gonçalves, C.I.; Al-Naama, A.; Saraiva, L.R.; Lemos, M.C.
A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism. Int. J. Mol. Sci. 2022, 23, 4423.
https://doi.org/10.3390/ijms23084423
AMA Style
Fadiga L, Lavrador M, Vicente N, Barros L, Gonçalves CI, Al-Naama A, Saraiva LR, Lemos MC.
A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism. International Journal of Molecular Sciences. 2022; 23(8):4423.
https://doi.org/10.3390/ijms23084423
Chicago/Turabian Style
Fadiga, Lúcia, Mariana Lavrador, Nuno Vicente, LuÃsa Barros, Catarina I. Gonçalves, Asma Al-Naama, Luis R. Saraiva, and Manuel C. Lemos.
2022. "A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism" International Journal of Molecular Sciences 23, no. 8: 4423.
https://doi.org/10.3390/ijms23084423
APA Style
Fadiga, L., Lavrador, M., Vicente, N., Barros, L., Gonçalves, C. I., Al-Naama, A., Saraiva, L. R., & Lemos, M. C.
(2022). A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism. International Journal of Molecular Sciences, 23(8), 4423.
https://doi.org/10.3390/ijms23084423