<i>GATA6</i> mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrumDoris Škorić‐Milosavljević, Alex V. Postma, Daniela Q.C.M. Barge‐Schaapveld et al.|American Journal of Medical Genetics Part A|2019Cited by 28
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
Reduced kinase function in two ultra‐rare <scp> <i>TNNI3K</i> </scp> variants in families with congenital junctional ectopic tachycardiaCaroline Pham, Elisabeth M. Lodder, Tamara T. Koopmann et al.|Clinical Genetics|2024Cited 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
Author response for "Reduced kinase function in two ultra‐rare <scp><i>TNNI3K</i></scp> variants in families with congenital junctional ectopic tachycardia"Caroline Pham, Elisabeth M. Lodder, Tamara T. Koopmann et al.|Unknown|2024Cited by 0