(Q58666635)
Statements
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted (English)
R Weksberg
I Teshima
C R Greenberg
S M Pueschel
J E Chernos
S B Fowlow
I J Anderson