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Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome. door Hempel, A, Pagnamenta, A, Blyth, M, Mansour, S, McConnell, V, Kou, I, Ikegawa, S, Tsurusaki, Y, Matsumoto, N, Lo-Castro, A, Plessis, G, Albrecht, B, Battaglia, A, Taylor, J, Howard, M, Keays, D, Sohal, A, Kühl, S, Kini, U, McNeill, A
Gepubliceerd in 2015Journal article -
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A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups. door Londono, D, Kou, I, Johnson, T, Sharma, S, Ogura, Y, Tsunoda, T, Takahashi, A, Matsumoto, M, Herring, J, Lam, T, Wang, X, Tam, E, Song, Y, Fan, Y, Chan, D, Cheah, K, Qiu, X, Jiang, H, Huang, D, TSRHC IS Clinical Group, International Consortium for Scoliosis Genetics, Su, P, Sham, P, Cheung, K, Luk, K
Gepubliceerd in 2014Journal article