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http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_26/101093hmg10262989/authorship/11
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http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_26/101093hmg10262989/affiliation/AFF1
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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
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