bibliographicCitation |
Fregeau B, Kim B, Hernández-García A, Jordan V, Cho M, Schnur R, Monaghan K, Juusola J, Rosenfeld J, Bhoj E, Zackai E, Sacharow S, Barañano K, Bosch DM, de Vries BA, Lindstrom K, Schroeder A, James P, Kulch P, Lalani S, van Haelst M, van Gassen KI, van Binsbergen E, Barkovich A , Scott D, Sherr E. De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions. The American Journal of Human Genetics. 2016 May;98(5):963–70. doi: 10.1016/j.ajhg.2016.03.002. |