High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia - Nik-Zainal, S; Strick, R; Storer, M; Huang, N; Rad, R; Willatt, L; Fitzgerald, T; Martin, V; Sandford, R; Carter, N P; Janecke, A R; Renner, S P; Oppelt, P G; Oppelt, P; Schulze, C; Brucker, S; Hurles, M; Beckmann, M W; Strissel, P L; Shaw-Smith, C (J Med Genet, 2011)