Showing 1 - 6 results of 6 for search 'Vermeesch, JR', query time: 0.03s
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1
Current controversies in prenatal diagnosis 3: Gene editing should replace embryo selection following PGD by Wells, D, Vermeesch, JR, Simpson, JL
Published 2019Journal article -
2
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. by Hannes, F, Sharp, A, Mefford, H, de Ravel, T, Ruivenkamp, C, Breuning, M, Fryns, J, Devriendt, K, Van Buggenhout, G, Vogels, A, Stewart, H, Hennekam, R, Cooper, G, Regan, R, Knight, S, Eichler, E, Vermeesch, JR
Published 2009Journal article -
3
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant by Hannes, F, Sharp, A, Mefford, H, de Ravel, T, Ruivenkamp, C, Breuning, M, Fryns, J, Devriendt, K, Van Buggenhout, G, Vogels, A, Stewart, H, Hennekam, R, Cooper, G, Regan, R, Knight, S, Eichler, E, Vermeesch, JR
Published 2009Journal article -
4
Valproic acid confers functional pluripotency to human amniotic fluid stem cells in a transgene-free approach by Moschidou, D., Mukherjee, S., Blundell, M.P., Drews, K., Jones, G.N., Abdulrazzak, H., Nowakowska, B., Phoolchund, A., Lay, K., Ramasamy, T.S., Cananzi, M., Nettersheim, D., Sullivan, M., Frost, J., Moore, G., Vermeesch, J.R., Fisk, N.M., Thrasher, A.J., Atala, A., Adjaye, J., Schorle, H., De Coppi, P., Guillot, P.V.
Published 2012Article -
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The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists by Sermon, K, Capalbo, A, Cohen, J, Coonen, E, De Rycke, M, De Vos, A, Delhanty, J, Fiorentino, F, Gleicher, N, Griesinger, G, Grifo, J, Handyside, A, Harper, J, Kokkali, G, Mastenbroek, S, Meldrum, D, Meseguer, M, Montag, M, Munné, S, Rienzi, L, Rubio, C, Scott, K, Scott, R, Simon, C, Swain, J, Treff, N, Ubaldi, F, Vassena, R, Vermeesch, JR, Verpoest, W, Wells, D, Geraedts, J
Published 2016Journal article -
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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome by Davies, RW, Fiksinski, AM, Breetvelt, EJ, Williams, NM, Hooper, SR, Monfeuga, T, Bassett, AS, Owen, MJ, Gur, RE, Morrow, BE, McDonald-McGinn, DM, Swillen, A, Chow, EWC, van den Bree, M, Emanuel, BS, Vermeesch, JR, van Amelsvoort, T, Arango, C, Armando, M, Campbell, LE, Cubells, JF, Eliez, S, Garcia-Minaur, S, Gothelf, D, Kates, WR, Murphy, KC, Murphy, CM, Murphy, DG, Philip, N, Repetto, GM, Shashi, V, Simon, TJ, Suñer, DH, Vicari, S, Scherer, SW, Bearden, CE, Vorstman, JAS, International 22q11.2 Brain and Behavior Consortium
Published 2020Journal article