एपीए उद्धरण

Cappuccio, G., Brunetti‐Pierri, R., Torella, A., Pinelli, M., Castello, R., Casari, G., . . . Brunetti‐Pierri, N. (2019). Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4. Mol Genet Genomic Med.

शिकागो स्टाइल उद्धरण

Cappuccio, Gerarda, et al. "Retinal Dystrophy in an Individual Carrying a De Novo Missense Variant of SMARCA4." Mol Genet Genomic Med 2019.

एमएलए उद्धरण

Cappuccio, Gerarda, et al. "Retinal Dystrophy in an Individual Carrying a De Novo Missense Variant of SMARCA4." Mol Genet Genomic Med 2019.