RET gene mutations are not a common cause of congenital solitary functioning kidney in adults

por Oram, Richard A., Edghill, Emma L., Woolf, Adrian S., Hennekam, R. C., Ellard, Sian, Hattersley, A. T., Bingham, Coralie
Publicado 2009

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

por Hannes, F D, Sharp, A J, Mefford, H C, de Ravel, T, Ruivenkamp, C A, Breuning, M H, Fryns, J-P, Devriendt, K, Van Buggenhout, G, Vogels, A, Stewart, H, Hennekam, R C, Cooper, G M, Regan, R, Knight, S J L, Eichler, E E, Vermeesch, J R
Publicado 2009