(Q40761872)
Statements
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Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1. (English)
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Weksberg R
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Nishikawa J
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Caluseriu O
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Fei YL
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Shuman C
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Wei C
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Steele L
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Cameron J
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Smith A
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Ambus I
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Li M
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Ray PN
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Sadowski P
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Squire J
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1 December 2001
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10
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26
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2989-3000
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Identifiers
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