Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2 von LIGTENBERG, M. J. L, HOGERVORST, F. B. L, VOS, E. M. A. W, WIGBOUT, G, STRUYCKEN, P. M, MENKO, F. H, RUTGERS, E. J. T, HOEFSLOOT, E. H, MARIMAN, E. C. M, BRUNNER, H. G, VAN'T VEER, L. J, WILLEMS, H. W, ARTS, P. J. W, BRINK, G, HAGEMAN, S, BOSGOED, E. A. J, VAN DER LOOIJ, E, ROOKUS, M. A, DEVILEE, P

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Genome sequencing as a generic diagnostic strategy for rare disease von Schobers, Gaby, Derks, Ronny, den Ouden, Amber, Swinkels, Hilde, van Reeuwijk, Jeroen, Bosgoed, Ermanno, Lugtenberg, Dorien, Sun, Su Ming, Corominas Galbany, Jordi, Weiss, Marjan, Blok, Marinus J, Olde Keizer, Richelle A C M, Hofste, Tom, Hellebrekers, Debby, de Leeuw, Nicole, Stegmann, Alexander, Kamsteeg, Erik-Jan, Paulussen, Aimee D C, Ligtenberg, Marjolijn J L, Bradley, Xiangqun Zheng, Peden, John, Gutierrez, Alejandra, Pullen, Adam, Payne, Tom, Gilissen, Christian, van den Wijngaard, Arthur, Brunner, Han G, Nelen, Marcel, Yntema, Helger G, Vissers, Lisenka E L M

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PTEN mutation in a family with Cowden syndrome and autism von Goffin, Aleide, Hoefsloot, Lies H., Bosgoed, Ermanno, Swillen, Ann, Fryns, Jean-Pierre

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Additional file 1 of Genome sequencing as a generic diagnostic strategy for rare disease von Schobers, Gaby, Derks, Ronny, den Ouden, Amber, Swinkels, Hilde, van Reeuwijk, Jeroen, Bosgoed, Ermanno, Lugtenberg, Dorien, Sun, Su Ming, Corominas Galbany, Jordi, Weiss, Marjan, Blok, Marinus J., Olde Keizer, Richelle A. C. M., Hofste, Tom, Hellebrekers, Debby, de Leeuw, Nicole, Stegmann, Alexander, Kamsteeg, Erik-Jan, Paulussen, Aimee D. C., Ligtenberg, Marjolijn J. L., Bradley, Xiangqun Zheng, Peden, John, Gutierrez, Alejandra, Pullen, Adam, Payne, Tom, Gilissen, Christian, van den Wijngaard, Arthur, Brunner, Han G., Nelen, Marcel, Yntema, Helger G., Vissers, Lisenka E. L. M.

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