AAAAAA

   
Results: 1-3 |
Results: 3

Authors: Hagan, DM Ross, AJ Strachan, T Lynch, SA Ruiz-Perez, V Wang, YM Scambler, P
Citation: Dm. Hagan et al., Mutation analysis and embryonic expression of the HLXB9 Currarino syndromegene (vol 66, pg 1504, 2000), AM J HU GEN, 67(3), 2000, pp. 769-769

Authors: Hagan, DM Ross, AJ Strachan, T Lynch, SA Ruiz-Perez, V Wang, YM Scambler, P Custard, E Reardon, W Hassan, S Muenke, M Nixon, P Papapetrou, C Winter, RM Edwards, Y Morrison, K Barrow, M Cordier-Alex, MP Correia, P Galvin-Parton, PA Gaskill, S Gaskin, KJ Garcia-Minaur, S Gereige, R Hayward, R Homfray, T McKeown, C Murday, V Plauchu, H Shannon, N Spitz, L Lindsay, S
Citation: Dm. Hagan et al., Mutation analysis and embryonic expression of the HLXB9 Currarino syndromegene, AM J HU GEN, 66(5), 2000, pp. 1504-1515

Authors: Sakuntabhai, A Ruiz-Perez, V Carter, S Jacobsen, N Burge, S Monk, S Smith, M Munro, CS O'Donovan, M Craddock, N Kucherlapati, R Rees, JL Owen, M Lathrop, GM Monaco, AP Strachan, T Hovnanian, A
Citation: A. Sakuntabhai et al., Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease, NAT GENET, 21(3), 1999, pp. 271-277
Risultati: 1-3 |