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Basic genetics concepts: Chromosomes and cell division
Basic genetics concepts: DNA regulation and gene expression
Genetics: Glossary of terms
Genomic disorders: An overview
Inheritance patterns of monogenic disorders (Mendelian and non-Mendelian)
Mitochondrial structure, function, and genetics
Overview of gene therapy, gene editing, and gene silencing
Overview of stem cells
Principles of complex trait genetics
Principles of epigenetics
Genetic counseling: Family history interpretation and risk assessment
Genetic testing
Personalized medicine
Secondary findings from genetic testing
Arrhythmogenic right ventricular cardiomyopathy: Pathogenesis and genetics
Autosomal dominant polycystic kidney disease (ADPKD): Genetics of the disease and mechanisms of cyst growth
Autosomal recessive polycystic kidney disease in children
Charcot-Marie-Tooth disease: Genetics, clinical features, and diagnosis
Classification of diabetes mellitus and genetic diabetic syndromes
Classification, cytogenetics, and molecular genetics of acute lymphoblastic leukemia/lymphoma
Clinical manifestations, diagnosis, and natural history of alpha-1 antitrypsin deficiency
Congenital long QT syndrome: Pathophysiology and genetics
Cystic fibrosis: Genetics and pathogenesis
Dravet syndrome: Genetics, clinical features, and diagnosis
Duchenne and Becker muscular dystrophy: Genetics and pathogenesis
Eosinophilic esophagitis (EoE): Genetics and immunopathogenesis
Familial Mediterranean fever: Epidemiology, genetics, and pathogenesis
Focal segmental glomerulosclerosis: Genetic causes
Genetic disorders of the collecting tubule sodium channel: Liddle's syndrome and pseudohypoaldosteronism type 1
Genetic factors in inflammatory bowel disease
Genetic factors in the pathogenesis of hypertension
Genetic risk factors for prostate cancer
Genetics and clinical presentation of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Genetics and clinical presentation of nonclassic (late-onset) congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Genetics and pathophysiology of glucose-6-phosphate dehydrogenase (G6PD) deficiency
Genetics of Alzheimer disease
Genetics of asthma
Genetics of dilated cardiomyopathy
Genetics of hemophilia A and B
Genetics, clinical features, and diagnosis of Marfan syndrome and related disorders
Genetics, pathogenesis, and pathology of Alport syndrome (hereditary nephritis)
HFE and other hemochromatosis genes
Huntington disease: Genetics and pathogenesis
Hypertrophic cardiomyopathy: Gene mutations and clinical genetic testing
Molecular genetics of colorectal cancer
Molecular genetics of the thalassemia syndromes
Overview of hereditary breast and ovarian cancer syndromes associated with genes other than BRCA1/2
Pathogenesis of idiopathic pulmonary fibrosis
Peptide hormone signal transduction and regulation
Personalized medicine
Primary ciliary dyskinesia (immotile-cilia syndrome)
Rett syndrome: Genetics, clinical features, and diagnosis
Tuberous sclerosis complex: Genetics, clinical features, and diagnosis
Unipolar depression: Genetics
Genetic association and GWAS studies: Principles and applications
Mendelian randomization
Next-generation DNA sequencing (NGS): Principles and clinical applications
Tools for genetics and genomics: Cytogenetics and molecular genetics
Tools for genetics and genomics: Gene expression profiling
Tools for genetics and genomics: Model systems
Tools for genetics and genomics: Polymerase chain reaction
Tools for genetics and genomics: Specially bred and genetically engineered mice
Overview of pharmacogenomics