(Q24679370)

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Uniparental disomy as a mechanism for human genetic disease

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Uniparental disomy as a mechanism for human genetic disease (English)
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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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February 1988
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42
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2
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217-26
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