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:
Papapetrou, C
Drummond, F
Reardon, W
Winter, R
Spitz, L
Edwards, YH
Citation: C. Papapetrou et al., A genetic study of the human T gene and its exclusion as a major candidategene for sacral agenesis with anorectal atresia, J MED GENET, 36(3), 1999, pp. 208-213
Authors:
Wadey, R
McKie, J
Papapetrou, C
Sutherland, H
Lohman, F
Osinga, J
Frohn, I
Hofstra, R
Meijers, C
Amati, F
Conti, E
Pizzuti, A
Dallapiccola, B
Novelli, G
Scambler, P
Citation: R. Wadey et al., Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11, AM J HU GEN, 65(1), 1999, pp. 247-249