ADGC Publications

Found 1 results
Filters: Author is Samocha, Kaitlin E and Keyword is Child Development Disorders, Pervasive  [Clear All Filters]
2014
Samocha KE, Robinson EB, Sanders SJ, Stevens C, Sabo A, McGrath LM, Kosmicki JA, Rehnström K, Mallick S, Kirby A et al..  2014.  A framework for the interpretation of de novo mutation in human disease.. Nat Genet. 46(9):944-50.