Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.

Koolen, Da; Sharp, Aj; Hurst, Ja; Firth, Hv; Knight, Sj; Goldenberg, A; SAUGIER VEBER, P; Pfundt, R; Vissers, Le; Destrée, A; Grisart, B; Rooms, L; VAN DER AA, N; Field, M; Hackett, A; Bell, K; Nowaczyk, Mj; Mancini, Gm; Poddighe, Pj; Schwartz, Ce; Rossi, Elena; DE GREGORI, Manuela; ANTONACCI FULTON, Ll; MCLELLAN MD, Nd; Garrett, Jm; Wiechert, Ma; Miner, Tl; Crosby, S; Ciccone, Roberto; Willatt, L; Rauch, A; Zenker, M; Aradhya, S; Manning, Ma; Strom, Tm; Wagenstaller, J; KREPISCHI SANTOS, Ac; VIANNA MORGANTE, Am; Rosenberg, C; Price, Sm; Stewart, H; SHAW SMITH, C; Brunner, Hg; Wilkie, Ao; Veltman, Ja; Zuffardi, Orsetta; Eichler, Ee; DE VRIES, Bb