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Methods in Molecular Medicine|August 26, 2006
Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia using denaturing high-performance liquid chromatography and sequencingAlex V Postma, Zahurul A Bhuiyan, Hennie BikkerAdvances in Experimental Medicine and Biology|June 17, 2024
Molecular Pathways and Animal Models of Ebstein's AnomalyBjarke Jensen, Gregor U Andelfinger, Alex V PostmaCardiovascular Research|May 14, 2011
Developmental aspects of cardiac arrhythmogenesisAlex V Postma, Vincent M Christoffels, Connie R BezzinaJournal of Human Genetics|July 31, 2015
Genetics of congenital heart disease: the contribution of the noncoding regulatory genomeAlex V Postma, Connie R Bezzina, Vincent M ChristoffelsDisease Models & Mechanisms|May 17, 2023
Genetics of sinoatrial node function and heart rate disordersLieve E van der Maarel, Alex V Postma, Vincent M ChristoffelsTrends in Cardiovascular Medicine|October 13, 2009
Developmental and genetic aspects of atrial fibrillationAlex V Postma, Lukas R C Dekker, Alexandre T Soufan, et al.Pacing and Clinical Electrophysiology : PACE|August 8, 2008
A case of catecholaminergic polymorphic ventricular tachycardia caused by two calsequestrin 2 mutationsSam de la Fuente, Irene M Van Langen, Alex V Postma, et al.American Journal of Medical Genetics. Part A|May 29, 2020
Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiencyEline A Verberne, Sonja Faries, Marcel M A M Mannens, et al.Molecular Genetics & Genomic Medicine|February 6, 2019
Identifying pathogenic variants in the Follistatin-like 1 gene (FSTL1) in patients with skeletal and atrioventricular valve disordersStuti Prakash, Andrea Mattiotti, Marc Sylva, et al.American Journal of Medical Genetics. Part A|May 23, 2013
The value of the clinical geneticist caring for adults with congenital heart disease: diagnostic yield and patients' perspectiveKlaartje van Engelen, Marieke J H Baars, Joyce P Felix, et al.Pageof 7