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Publications by Emily E. Brown
Protein Molecular Modeling Techniques Investigating Novel TAB2 Variant R347X Causing Cardiomyopathy and Congenital Heart Defects in Multigenerational Family
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Magnetic and Structural Characterization of Ultra-Thin Fe (222) Films
AIP Advances
Nanotechnology
Astronomy
Physics
Nanoscience
Related publications
Imaging Techniques for Visualizing and Phenotyping Congenital Heart Defects in Murine Models
Birth Defects Research Part C - Embryo Today: Reviews
Medicine
Embryology
Developmental Biology
A Systematic Variant Screening in Familial Cases of Congenital Heart Defects Demonstrates the Usefulness of Molecular Genetics in This Field
European Journal of Human Genetics
Genetics
Copy Number Variation in Congenital Heart Defects
Current Genetic Medicine Reports
Recurrence of Congenital Heart Defects in Families
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Comprehensive Approach to Congenital Heart Defects
Journal of Cardiovascular Disease Research
Cardiovascular Medicine
Cardiology
Congenital Anomalies in the Heart With Hypertrophic Cardiomyopathy.
Heart
Cardiovascular Medicine
Cardiology
MESP1 Mutations in Patients With Congenital Heart Defects
Human Mutation
Genetics
A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family With Dilated Cardiomyopathy (FDCM)
PLoS ONE
Multidisciplinary
Extracardiac Defects in Children With Congenital Heart Disease.
Heart
Cardiovascular Medicine
Cardiology
