Feil Family Brain & Mind Research Institute

Publications

Found 1 results
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Filters: Keyword is Mutagenesis, Site-Directed and Author is Giamanco, Kristin A  [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.