Breaking up rationally by Villiger, D, de Vries, B

Volcano instability induced by strike-slip faulting by Lagmay, A, de Vries, B, Kerle, N, Pyle, D

Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype? by De Vries, B, Knight, S, Homfray, T, Smithson, S, Flint, J, Winter, R

Forging links between human mental retardation-associated CNVs and mouse gene knockout models. by Webber, C, Hehir-Kwa, J, Nguyen, D, de Vries, B, Veltman, J, Ponting, C

Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13). by de Vries, B, Lees, M, Knight, S, Regan, R, Corney, D, Flint, J, Barnicoat, A, Winter, R

A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome. by de Vries, B, Bitner-Glindzicz, M, Knight, S, Tyson, J, MacDermont, K, Flint, J, Malcolm, S, Winter, R

Accurate distinction of pathogenic from benign CNVs in mental retardation. by Hehir-Kwa, J, Wieskamp, N, Webber, C, Pfundt, R, Brunner, H, Gilissen, C, de Vries, B, Ponting, C, Veltman, J

Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders by Van Der Donk, R, Jansen, S, Schuurs-Hoeijmakers, J, Koolen, D, Goltstein, L, Hoischen, A, Brunner, H, Kemmeren, P, Nellaker, C, Vissers, L, De Vries, B, Hehir-Kwa, J

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist. by de Vries, B, White, S, Knight, S, Regan, R, Homfray, T, Young, I, Super, M, McKeown, C, Splitt, M, Quarrell, O, Trainer, A, Niermeijer, M, Malcolm, S, Flint, J, Hurst, J, Winter, R

Characterization of a recurrent 15q24 microdeletion syndrome. by Sharp, A, Selzer, R, Veltman, J, Gimelli, S, Gimelli, G, Striano, P, Coppola, A, Regan, R, Price, S, Knoers, N, Eis, P, Brunner, H, Hennekam, R, Knight, S, de Vries, B, Zuffardi, O, Eichler, E

Clinical significance of de novo and inherited copy-number variation. by Vulto-van Silfhout, A, Hehir-Kwa, J, van Bon, B, Schuurs-Hoeijmakers, J, Meader, S, Hellebrekers, C, Thoonen, I, de Brouwer, A, Brunner, H, Webber, C, Pfundt, R, de Leeuw, N, de Vries, B

Clinical Significance of De Novo and Inherited Copy-Number Variation by Vulto-van Silfhout, A, Hehir-Kwa, J, van Bon, B, Schuurs-Hoeijmakers, J, Meader, S, Hellebrekers, C, Thoonen, I, de Brouwer, A, Brunner, H, Webber, C, Pfundt, R, de Leeuw, N, De Vries, B

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

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications. by 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

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