Found: 8
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Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2021, v. 59, n. 5, p. 955, doi. 10.1515/cclm-2020-1318
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- Publication type:
- Article
Characterization of the cHS4 insulator in mouse embryonic stem cells.
- Published in:
- FEBS Open Bio, 2020, v. 10, n. 4, p. 644, doi. 10.1002/2211-5463.12818
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- Publication type:
- Article
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 408, doi. 10.3390/genes12030408
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- Publication type:
- Article
HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 3, p. 547, doi. 10.1007/s00246-016-1547-8
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- Publication type:
- Article
Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions.
- Published in:
- Biology (2079-7737), 2022, v. 11, n. 4, p. 489, doi. 10.3390/biology11040489
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- Publication type:
- Article
Can Time-Lapse Incubation and Monitoring Be Beneficial to Assisted Reproduction Technology Outcomes? A Randomized Controlled Trial Using Day 3 Double Embryo Transfer.
- Published in:
- Frontiers in Physiology, 2022, v. 12, p. 1, doi. 10.3389/fphys.2021.794601
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- Publication type:
- Article
KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.
- Published in:
- 2022
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- Publication type:
- journal article
PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.
- Published in:
- 2021
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- Publication type:
- journal article