Uniparental disomy as a mechanism for human genetic disease (Q24679370)
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(P1476) "Uniparental disomy as a mechanism for human genetic disease" (language: en)

(P2093) J E Spence
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R G Perciaccante
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G M Greig
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H F Willard
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D H Ledbetter
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J F Hejtmancik
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M S Pollack
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W E O'Brien
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A L Beaudet
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