Weksberg R. et al. 1993
Weksberg R., Teshima I., Williams B.R., Greenberg C.R., Pueschel S.M., Chernos J.E., Fowlow S.B., Hoyme E., Anderson I.J., Whiteman D.A., et al., 1993. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. Hum. Mol. Genet. 2: 549-556.
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