(Q46166434)
Statements
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Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis (English)
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B H W Faas
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I van der Burgt
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A J A Kooper
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R Pfundt
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J Y Hehir-Kwa
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A P T Smits
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N de Leeuw
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24 June 2010
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47
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9
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586-594
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Identifiers
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