AAAAAA

   
Results: 1-5 |
Results: 5

Authors: Schurman, SJ Perlman, SA Sutphen, R Campos, A Garin, EH Cruz, DN Shoemaker, LR
Citation: Sj. Schurman et al., Genotype/phenotype observations in African Americans with Bartter syndrome, J PEDIAT, 139(1), 2001, pp. 105-110

Authors: Risler, EA Sutphen, R Shields, J
Citation: Ea. Risler et al., Preliminary validation of the juvenile first offender risk assessment index, RES SOC W P, 10(1), 2000, pp. 111-126

Authors: Nowak, KJ Wattanasirichaigoon, D Goebel, HH Wilce, M Pelin, K Donner, K Jacob, RL Hubner, C Oexle, K Anderson, JR Verity, CM North, KN Iannaccone, ST Muller, CR Nurnberg, P Muntoni, F Sewry, C Hughes, I Sutphen, R Lacson, AG Swoboda, KJ Vigneron, J Wallgren-Pettersson, C Beggs, AH Laing, NG
Citation: Kj. Nowak et al., Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy, NAT GENET, 23(2), 1999, pp. 208-212

Authors: Sutphen, R Diamond, TM Minton, SE Peacocke, M Tsou, HC Root, AW
Citation: R. Sutphen et al., Severe Lhermitte-Duclos disease with unique germline mutation of PTEN, AM J MED G, 82(4), 1999, pp. 290-293

Authors: Bamshad, M Le, T Watkins, WS Dixon, ME Kramer, BE Roeder, AD Carey, JC Root, S Schinzel, A Van Maldergem, L Gardner, RJM Lin, RC Seidman, CE Seidman, JG Wallerstein, R Moran, E Sutphen, R Campbell, CE Jorde, LB
Citation: M. Bamshad et al., The spectrum of mutations in TBX3: Genotype phenotype relationship in ulnar-mammary syndrome, AM J HU GEN, 64(6), 1999, pp. 1550-1562
Risultati: 1-5 |