CNV-WebStore: Online CNV Analysis, Storage and Interpretation by Wuyts Wim, Reyniers Edwin, Vandeweyer Geert, Rooms Liesbeth, Kooy R Frank

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Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches. by 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. by 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

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. by Jacquemont, S, Reymond, A, Zufferey, F, Harewood, L, Walters, R, Kutalik, Z, Martinet, D, Shen, Y, Valsesia, A, Beckmann, N, Thorleifsson, G, Belfiore, M, Bouquillon, S, Campion, D, de Leeuw, N, de Vries, B, Esko, T, Fernandez, B, Fernández-Aranda, F, Fernández-Real, J, Gratacòs, M, Guilmatre, A, Hoyer, J, Jarvelin, MR, Kooy, R

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus by Jacquemont, S, Reymond, A, Zufferey, F, Harewood, L, Walters, R, Kutalik, Z, Martinet, D, Shen, Y, Valsesia, A, Beckmann, N, Thorleifsson, G, Belfiore, M, Bouquillon, S, Campion, D, de Leeuw, N, de Vries, B, Esko, T, Fernandez, B, Fernández-Aranda, F, Fernández-Real, J, Gratacòs, M, Guilmatre, A, Hoyer, J, Jarvelin, M, Frank Kooy, R