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Journal of Cardiovascular Electrophysiology|August 2, 2007
A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22Zahurul A Bhuiyan, Mohamed A Hamdan, Eman T A Shamsi, et al.
Journal of Molecular and Cellular Cardiology|March 23, 2010
The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handlingUwe Kirchhefer, Diana Wehrmeister, Alex V Postma, et al.
Circulation Research|October 19, 2002
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardiaAlex V Postma, Isabelle Denjoy, Theo M Hoorntje, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|May 18, 2012
The clinical and molecular relations between idiopathic preterm labor and maternal congenital heart defectsMonique W M de Laat, Petronella G Pieper, Martijn A Oudijk, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 25, 2013
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7Alexa M C Vermeer, Klaartje van Engelen, Alex V Postma, et al.
Plos One|September 18, 2012
Identifying the evolutionary building blocks of the cardiac conduction systemBjarke Jensen, Bastiaan J D Boukens, Alex V Postma, et al.
American Journal of Medical Genetics. Part A|August 8, 2014
A mutation in the Kozak sequence of GATA4 hampers translation in a family with atrial septal defectsRajiv A Mohan, Klaartje van Engelen, Sonia Stefanovic, et al.
Fetal Diagnosis and Therapy|June 7, 2014
Bicuspid aortic valve morphology and associated cardiovascular abnormalities in fetal Turner syndrome: a pathomorphological studyKlaartje van Engelen, Margot M Bartelings, Adriana C Gittenberger-de Groot, et al.
Epigenomics|March 16, 2019
DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypesJan Maarten Cobben, Izabela M Krzyzewska, Andrea Venema, et al.
Heart (British Cardiac Society)|April 2, 2010
22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresiaKlaartje van Engelen, Ana Topf, Bernard D Keavney, et al.
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