Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation (Q24681734)
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Current Data About Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation
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(P1476) "Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation" (language: en)

(P2093) W W Lam
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I Hatada
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S Ohishi
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T Mukai
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J A Joyce
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T R Cole
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D Donnai
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P N Schofield
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E R Maher
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