(Q43073791)
Statements
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Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients (English)
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Reis A
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Rauch A
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Devriendt K
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Koch A
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Rauch R
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Gewillig M
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Kraus C
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Weyand M
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Singer H
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Hofbeck M
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Identifiers
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