Feil Family Brain & Mind Research Institute

Publications

Found 1 results
Author Title Type [ Year(Asc)]
Filters: Author is Schwartzentruber, Jeremy and Keyword is Abnormalities, Multiple  [Clear All Filters]
2014
Mirzaa G, Parry DA, Fry AE, Giamanco KA, Schwartzentruber J, Vanstone M, Logan CV, Roberts N, Johnson CA, Singh S et al..  2014.  De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.. Nat Genet. 46(5):510-515.