Search results - ORA - Oxford University Research Archive

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1

Journal article

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Sifrim, A, Hitz, M, Wilsdon, A, et al.
2016-08-01

2

Journal article

Rare variants in NR2F2 cause congenital heart defects in humans.

Al Turki, S, Manickaraj, A, Mercer, C, et al.
2014-04-01

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