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Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of FallotDoris Škorić‐Milosavljević, Sally‐Ann B. Clur, Najim Lahrouchi et al.|Genetics in Medicine|2021Cited by 17
Genetic Burden of <i>TNNI3K</i> in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular ArrhythmiasCaroline Pham, Elisabeth M. Lodder, Karolina Andrzejczyk et al.|Circulation Genomic and Precision Medicine|2023Cited by 5
Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of FallotDoris Škorić‐Milosavljević, Sally‐Ann B. Clur, Najim Lahrouchi et al.|Genetics in Medicine|2021Cited by 0