Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour
- 期刊名称Human Molecular Genetics
- 作者Sparago, A.; Russo, S.; Cerrato, F.; Ferraiuolo, S.; Castorina, P.; Selicorni, A.; Schwienbacher, C.; Negrini, M.; Ferrero, G. B.; Silengo, M. C.; Anichini, C.; Larizza, L.; Riccio, A.
- 卷第16卷
- 期第3期
- 印刷ISSN0964-6906
- 电子ISSN1460-2083
- 文件大小571.09KB
- 发表时间2006-12-21
- DOI10.1093/hmg/ddl448
- 页码254-264
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at 8 GeV/ <i>c</i>Abashian, A.; Eisenstein, B.; Hansen, J. D.; Mollet, W.; Morris, G. R.; Nelson, B.; O'Halloran, T.; Orr, J. R.; Rhines, D.; Schultz, P.; Sokolsky, P.; Wagner, R. G.; Watson, J.; Gelfand, N. M.; Buttram, M. · Physical Review D · 1976
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