A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor.

Autor: Terenziani, Monica1, Sardella, Michele2, Gamba, Beatrice2, Testi, Maria Adele3, Spreafico, Filippo1, Ardissino, Gianluigi4, Fedeli, Fausto5, Fossati-Bellani, Franca1, Radice, Paolo2,6, Perotti, Daniela2 daniela.perotti@istitutotumori.mi.it
Zdroj: Pediatric Nephrology. Jul2009, Vol. 24 Issue 7, p1413-1417. 5p. 1 Color Photograph, 1 Graph.
Databáze: Academic Search Ultimate