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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Current Data About 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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(P1476) "Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted" (language: en)
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(P2093) R Weksberg
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I Teshima
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C R Greenberg
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S M Pueschel
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J E Chernos
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S B Fowlow
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I J Anderson
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D A Whiteman
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(P356) 10.1093/HMG/2.5.549
(P698) 8518793