Zada, A., Mundhofir, F. E. P., Pfundt, R., Leijsten, N., Nillesen, W., Faradz, S. M. H., & de Leeuw, N. (2014). 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. Hindawi Publishing Corporation.
Chicago Style CitationZada, Almira, Farmaditya E. P. Mundhofir, Rolph Pfundt, Nico Leijsten, Willy Nillesen, Sultana M. H. Faradz, i 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. Hindawi Publishing Corporation, 2014.
Cita MLAZada, 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. Hindawi Publishing Corporation, 2014.