Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
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Decoding Cryptogenic Cardioembolism
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Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
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Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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