Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted (Q58666635)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted |
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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