APA (7th ed.) Citation

Zada, A., Mundhofir, F. E. P., Pfundt, R., Leijsten, N., Nillesen, W., Faradz, S. M. H., & Leeuw, N. d. A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability. Wiley.

Chicago Style (17th ed.) Citation

Zada, Almira, Farmaditya E. P. Mundhofir, Rolph Pfundt, Nico Leijsten, Willy Nillesen, Sultana M. H. Faradz, and Nicole de Leeuw. A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability. Wiley.

MLA (9th ed.) Citation

Zada, Almira, et al. A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability. Wiley.