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Your search keyword '"Arndt, Anne-Karin"' showing total 8 results

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1. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

2. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

6. Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

8. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

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