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