|
XB--5799123
Papers associated with cc2d1a
???pagination.result.count???
???pagination.result.page??? 1
Sort Newest To Oldest | Sort Oldest To Newest |
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow., Kim AH, Sakin I, Viviano S, Tuncel G, Aguilera SM, Goles G, Jeffries L, Ji W, Lakhani SA, Kose CC, Silan F, Oner SS, Kaplan OI, MarmaRare Group, Ergoren MC, Mishra-Gorur K, Gunel M, Sag SO, Temel SG, Deniz E., Life Sci Alliance. October 21, 2024; 7 (10): ![]() |
???pagination.result.page??? 1