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7 results  for Everything in this catalogue

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Association Between Mutations in the NKX2.5 Homeobox, Atrial Septal Defects, Ventricular Noncompaction and Sudden Cardiac Death

Palomino Doza, Julián et al.

Revista española de cardiología. Volume 71:Number 1(2018); 201801; 53-55 -- Elsevier España, S.L.

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Abordaje de las cardiopatías familiares desde la Medicina genómica

Trujillo-Quintero, Juan Pablo et al.

Revista colombiana de cardiologia. Volume 25:Number 4 (2018, July); pp 264-276 -- Sociedad Colombiana de Cardiologia

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Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy: Growing Evidence

Roldán-Sevilla, Alvaro et al.

Circulation. Genomic and precision medicine. Volume 12:Number 3 (2019) -- Lippincott Williams & Wilkins

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Molecular Analysis of BMPR2, TBX4, and KCNK3 and Genotype-Phenotype Correlations in Spanish Patients and Families With Idiopathic and Hereditary Pulmonary Arterial Hypertension

Navas, Paula et al.

Revista española de cardiología. Volume 69:Number 11 (2016, November); pp 1011-1019 -- Elsevier España, S.L

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Variable Expressivity of a Founder Mutation in the EIF2AK4 Gene in Hereditary Pulmonary Veno-occlusive Disease and Its Impact on Survival

Navas Tejedor, Paula

Revista española de cardiología. Volume 71:Number 2 (2018, February); pp 86-94 -- Elsevier España, S.L

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Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations

Domínguez, Fernando et al.

Journal of the American College of Cardiology. Volume 72:Number 20 (2018, November 13th); pp 2471-2481 -- Elsevier Science

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Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy

Ochoa, Juan Pablo et al.

Journal of the American College of Cardiology. Volume 72:Number 20 (2018, November 13th); pp 2457-2467 -- Elsevier Science

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