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Mar Borregan

Autonomous University of Barcelona

15

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111

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P2253Risk of systemic embolisms in left ventricular noncompaction

2018 European Heart Journal
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P2250Role of family screening and genetic testing in left ventricular noncompaction

2018 European Heart Journal
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Comparative genomic hybridisation as a first option in genetic diagnosis: 1000 cases and a cost–benefit analysis

2018 Anales De Pediatria
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Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice

2018 European Journal of Human Genetics
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Array CGH como primera opción en el diagnóstico genético: 1.000 casos y análisis de coste-beneficio

2017 Anales De Pediatria
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3869Targeted next-generation sequencing as a comprehensive test for patients with hypertrophic cardiomyopathy

2017 European Heart Journal
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P6400Role of copy number variants in sudden cardiac death: genetic analysis and translation into clinical practice

2017 European Heart Journal
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A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region.

2015 Cytogenetic and Genome Research
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Enfermedad aórtica familiar no sindrómica: una entidad infradiagnosticada

2014 Revista Espanola De Cardiologia
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Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

2014 Clinica Chimica Acta
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Citations (14)