Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.
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L. Pasquier | S. Lyonnet | C. Gicquel | Y. Le Bouc | S. Chantot-Bastaraud | I. Netchine | S. Rossignol | S. Azzi | V. Steunou | N. Thibaud | B. Keren | M. Rossi | Walid Abi Habib | F. Brioude | C. Michot | Cristina Das Neves | M. Le Jule