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.

鸯铗痂蝈 蜞赕:

  • 蒿桡屙弪桕 BWS (耔礓痤 铃赈栩-妈溴爨磬)