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High-Throughput Identification of Causal Variants Underlying Cardiac Arrhythmia-Related GWAS Hits
The case of a 29-year-old woman with headaches and diplopia.
Recurrent Loss of Heterozygosity in Pancreatic Neuroendocrine Tumors.
Open-Source Inline Generative AI for Fast Cardiac MRI.
Region-specific expression of two mouse homeo box genes.
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Cardiovascular responses to PEEP and CPAP following repair of complicated congenital heart defects.
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Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice.
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[Surgery of congenital heart defects in deep hypothermic cardiovascular arrest: postoperative renal function].
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Enhanced desumoylation in murine hearts by overexpressed SENP2 leads to congenital heart defects and cardiac dysfunction.
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Haploinsufficiency of TAB2 causes congenital heart defects in humans.
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Intraoperative echocardiography for evaluation of congenital heart defects in infants and children.
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[Hydroxyproline in serum and urine in children with pulmonary hypertension in the course of congenital heart defects].
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Expression of sumoylation deficient Nkx2.5 mutant in Nkx2.5 haploinsufficient mice leads to congenital heart defects.
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S-100 after correction of congenital heart defects in neonates: is it a reliable marker for cerebral damage?
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The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model.
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Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
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[Atrial arrhythmias after modified Fontane operation: effect of preoperative hemodynamics and the kind of operation (atriopulmonary vs. total cavopulmonary anastomosis)].
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[Complex progressive palliation for univentricular circulation].
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[Echocardiographic diagnosis of the aorto-left ventricular tunnel].
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