APA (7th ed.) Citation

Elysa Jill Marco, Anne Brandes Aitken, Vishnu Prakas Nair, Gilberto da Gente, Molly Rae Gerdes, Leyla Bologlu, . . . Elliott H. Sherr. (2018). Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction. BMC.

Chicago Style (17th ed.) Citation

Elysa Jill Marco, Anne Brandes Aitken, Vishnu Prakas Nair, Gilberto da Gente, Molly Rae Gerdes, Leyla Bologlu, Sean Thomas, and Elliott H. Sherr. Burden of De Novo Mutations and Inherited Rare Single Nucleotide Variants in Children with Sensory Processing Dysfunction. BMC, 2018.

MLA (9th ed.) Citation

Elysa Jill Marco, et al. Burden of De Novo Mutations and Inherited Rare Single Nucleotide Variants in Children with Sensory Processing Dysfunction. BMC, 2018.