Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour
Cerrato, F., Sparago, A., Verde, G., De Crescenzo, A., Citro, V., Cubellis, M. V., Rinaldi, M. M., Boccuto, L., Neri, G., Magnani, C., D'Angelo, P., Collini, P., Perotti, D., Sebastio, G., Maher, E. RVolume:
17
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddn031
Date:
January, 2008
File:
PDF, 462 KB
english, 2008