Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
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G. Neri | L. Boccuto | M. Cubellis | E. Maher | G. Verde | A. Riccio | P. Collini | A. Sparago | F. Cerrato | D. Perotti | Valentina Citro | C. Magnani | P. D’Angelo | A. De Crescenzo | G. Sebastio | M. Rinaldi