(Q34091599)
Statements
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A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk (English)
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Evan E Eichler
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Maika Malig
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Jill A Rosenfeld
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Catarina D Campbell
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Blake C Ballif
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Santhosh Girirajan
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Brian Teague
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Laura Vives
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Lisa G Shaffer
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Tina A Graves
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Richard K Wilson
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David C Schwartz
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22 August 2010
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Identifiers
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