(Q52204453)
Statements
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Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. (English)
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Reik W
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Brown KW
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Schneid H
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Le Bouc Y
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Bickmore W
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Maher ER
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1 December 1995
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4
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2379-2385
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12
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Identifiers
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1 reference