Torthaí cuardaigh údar :: UTM Library Massive Scholar Tracking

1

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome. de réir 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

Foilsithe / Cruthaithe 2015

Journal article
2

A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups. de réir 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

Foilsithe / Cruthaithe 2014

Journal article