APA (7th ed.) Citation

Urakawa, T., Kanamaru, Y., Amano, N., Uchida, A., Fukami, M., & Kagami, M. Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith–Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region. BMC.

Chicago Style (17th ed.) Citation

Urakawa, Tatsuki, Yuri Kanamaru, Naoko Amano, Akira Uchida, Maki Fukami, and Masayo Kagami. Multi-locus Methylation Analyses Reveal GNAS Methylation Defects in Three Patients with the Beckwith–Wiedemann Syndrome Phenotype and No Molecular Defects in the 11p15.5 Imprinted Region. BMC.

MLA (9th ed.) Citation

Urakawa, Tatsuki, et al. Multi-locus Methylation Analyses Reveal GNAS Methylation Defects in Three Patients with the Beckwith–Wiedemann Syndrome Phenotype and No Molecular Defects in the 11p15.5 Imprinted Region. BMC.