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Results: 1-5 |
Results: 5

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 Putt, W Fox, M Edwards, YH
Citation: C. Papapetrou et al., The human TBX6 gene: Cloning and assignment to chromosome 16p11.2, GENOMICS, 55(2), 1999, pp. 238-241

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

Authors: Morrison, K Papapetrou, C Hol, FA Mariman, ECM Lynch, SA Burn, J Edwards, YH
Citation: K. Morrison et al., Susceptibility to spina bifida; an association study of five candidate genes, ANN HUM GEN, 62, 1998, pp. 379-396
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