Molecular and clinical delineation of the 17q22 microdeletion phenotype ‌ Laurell, T, Lundin, J, Nordenskjöld, A, Anderlid, B, Grigelioniene, G, Nordgren, A, Gorski, J, Knight, S, Krepischi, A, Price, S, Rosenberg, C, Vianna-Morgante, A, Turnpenny, P

Molecular and clinical delineation of the 17q22 microdeletion phenotype. ‌ Laurell, T, Lundin, J, Anderlid, B, Gorski, J, Grigelioniene, G, Knight, S, Krepischi, A, Nordenskjöld, A, Price, S, Rosenberg, C, Turnpenny, P, Vianna-Morgante, A, Nordgren, A

Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches. ‌ Koolen, D, Sistermans, E, Nilessen, W, Knight, S, Regan, R, Liu, Y, Kooy, R, Rooms, L, Romano, C, Fichera, M, Schinzel, A, Baumer, A, Anderlid, B, Schoumans, J, van Kessel, A, Nordenskjold, M, de Vries, B

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. ‌ Koolen, D, Vissers, L, Pfundt, R, de Leeuw, N, Knight, S, Regan, R, Kooy, R, Reyniers, E, Romano, C, Fichera, M, Schinzel, A, Baumer, A, Anderlid, B, Schoumans, J, Knoers, N, van Kessel, A, Sistermans, E, Veltman, J, Brunner, H, de Vries, B

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications. ‌ Wincent, J, Bruno, D, van Bon, B, Bremer, A, Stewart, H, Bongers, E, Ockeloen, C, Willemsen, M, Keays, D, Baird, G, Newbury, D, Kleefstra, T, Marcelis, C, Kini, U, Stark, Z, Savarirayan, R, Sheffield, L, Zuffardi, O, Slater, H, de Vries, B, Knight, S, Anderlid, B, Schoumans, J

Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome. ‌ Stewart, DR, Huang, A, Faravelli, F, Anderlid, B, Medne, L, Ciprero, K, Kaur, M, Rossi, E, Tenconi, R, Nordenskjöld, M, Gripp, K, Nicholson, L, Meschino, W, Capua, E, Quarrell, O, Flint, J, Irons, M, Giampietro, P, Schowalter, D, Zaleski, C, Malacarne, M, Zackai, E, Spinner, N, Krantz, I