Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

Por Liang, Y, Wang, A, Probst, F J, Arhya, I N, Barber, T D, Chen, K S, Deshmukh, D, Dolan, D F, Hinnant, J T, Carter, L E, Jain, P K, Lalwani, A K, Li, X C, Lupski, J R, Moeljopawiro, S, Morell, R, Negrini, C, Wilcox, E R, Winata, S, Camper, S A, Friedman, T B
Publicado em 1998

De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations

Por Probst, F. J., James, R. A., Burrage, L. C., Rosenfeld, J. A., Bohan, T. P., Melver, C. H. Ward, Magoulas, P., Austin, E., Franklin, A. I. A., Azamian, M., Xia, F., Patel, A., Bi, W., Bacino, C., Belmont, J.W., Ware, S. M., Shaw, C., Cheung, S.W., Lalani, S. R.
Publicado no Orphanet J Rare Dis (2015)