AAAAAA

   
Results: 1-3 |
Results: 3

Authors: Nishimura, DY Searby, CC Carmi, R Elbedour, K Van Maldergem, L Fulton, AB Lam, BL Powell, BR Swiderski, RE Bugge, KE Haider, NB Kwitek-Black, AE Ying, LH Duhl, DM Gorman, SW Heon, E Iannaccone, A Bonneau, D Biesecker, LG Jacobson, SG Stone, EM Sheffield, VC
Citation: Dy. Nishimura et al., Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2), HUM MOL GEN, 10(8), 2001, pp. 865-874

Authors: Pillers, DAH Fitzgerald, KM Duncan, NM Rash, SM White, RA Dwinnell, SJ Powell, BR Schnur, RE Ray, PN Cibis, GW Weleber, RG
Citation: Dah. Pillers et al., Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations, HUM GENET, 105(1-2), 1999, pp. 2-9

Authors: Shim, WKT Derieg, M Powell, BR Hsia, YE
Citation: Wkt. Shim et al., Near-total intestinal aganglionosis in the Waardenburg-Shah syndrome, J PED SURG, 34(12), 1999, pp. 1853-1855
Risultati: 1-3 |