The mouse Midl gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region

Dal Zotto, L; Quaderi, Na; Elliott, R; Lingerfelter, Pa; Carrel, L; Valsecchi, V; Montini, E; Yen, Ch; Chapman, V; Kalcheva, I; Arrigo, G; Zuffardi, Orsetta; Thomas, S; Willard, Hf; Ballabio, A; Disteche, Cm; Rugari, Ec