Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted
Title:
Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted
Author:
Weksberg, R. Teshima, I. Williams, B.R.G. Greenberg, C.R. Pueschel, S.M. Chernos, J.E. Fowlow, S.B. Hoyme, E. Anderson, I.J. Whiteman, D.A.H. Fisher, N. Squire, J.