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1. [p57.sup.KIP2] mutations associated with loss of IGF2 imprinting in Beckwith-Wiedemann syndrome

Author: Weksberg, R., Li, M., Fei, Y.L., Shuman, C., Chitayat, D., Atkin, J., Pauli, R.M., and Squire, J.A
Subjects: Genetic research -- Analysis, Human genetics -- Research, Beckwith-Wiedemann syndrome -- Genetic aspects, Biological sciences
Published: 2000

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