Boys duchenne muscular dystrophy muscular dystrophy emery dreifuss. Medical search. Frequent questions

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Anatomy11

Muscle, Skeletal Sarcolemma Muscle Fibers, Skeletal X Chromosome Muscles Myoblasts Diaphragm Chromosomes, Human, Pair 4 Satellite Cells, Skeletal Muscle Myoblasts, Skeletal Muscle Cells

Organisms4

Mice, Inbred mdx Mice, Inbred C57BL Dependovirus Mice, Transgenic

Diseases24

Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophy, Duchenne Muscular Dystrophies Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Neuromuscular Diseases Retinal Dystrophies Disease Models, Animal Cardiomyopathies Muscular Diseases Muscle Weakness Neuroaxonal Dystrophies Scoliosis Sarcoglycanopathies Walker-Warburg Syndrome Chromosome Deletion Syndrome Fibrosis Cardiomyopathy, Dilated

Chemicals and Drugs28

Thymopoietins Dystrophin Utrophin Sarcoglycans Dystroglycans Dystrophin-Associated Proteins Creatine Kinase Dystrophin-Associated Protein Complex Muscle Proteins Collagen Type VI Caveolin 3 Cytoskeletal Proteins Laminin Pregnenediones Morpholinos Lamin Type A Poly(A)-Binding Protein II Myostatin Membrane Proteins Glycerol Kinase Calpain Integrin alpha Chains Plectin Evans Blue Oligonucleotides, Antisense Nitric Oxide Synthase Type I Oligoribonucleotides, Antisense Connectin

Analytical, Diagnostic and Therapeutic Techniques and Equipment12

Heterozygote Detection Pedigree Genetic Therapy Disease Models, Animal Muscle Strength Prenatal Diagnosis Immunohistochemistry Chromosome Mapping DNA Mutational Analysis Biopsy Polymerase Chain Reaction Genetic Testing

Phenomena and Processes15

X Chromosome Exons Mutation Muscle Strength Regeneration Genetic Linkage Phenotype Chromosomes, Human, Pair 4 Heterozygote Muscle Development Genes, Recessive Chromosome Deletion Muscle Contraction Base Sequence Consanguinity

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Information Science2

Molecular Sequence Data Base Sequence

Health Care2

Genetic Counseling Genetic Testing

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science Health Care

Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophy, Duchenne Muscular Dystrophies Thymopoietins Muscular Dystrophy, Animal Dystrophin Mice, Inbred mdx Utrophin Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Sarcoglycans Muscle, Skeletal Dystroglycans Corneal Dystrophies, Hereditary Heterozygote Detection Muscular Dystrophy, Oculopharyngeal Dystrophin-Associated Proteins Sarcolemma Creatine Kinase Muscle Fibers, Skeletal X Chromosome Muscles Exons Pedigree Fuchs' Endothelial Dystrophy Myoblasts Dystrophin-Associated Protein Complex Muscle Proteins Neuromuscular Diseases Retinal Dystrophies Collagen Type VI Diaphragm Caveolin 3 Genetic Therapy Disease Models, Animal Cardiomyopathies Mutation Cytoskeletal Proteins Muscular Diseases Muscle Strength Regeneration Laminin Pregnenediones Genetic Linkage Phenotype Morpholinos Mice, Inbred C57BL Chromosomes, Human, Pair 4 Lamin Type A Poly(A)-Binding Protein II Heterozygote Muscle Development Dependovirus Satellite Cells, Skeletal Muscle Muscle Weakness Prenatal Diagnosis Myostatin Genes, Recessive Membrane Proteins Myoblasts, Skeletal Molecular Sequence Data Genetic Counseling Neuroaxonal Dystrophies Glycerol Kinase Immunohistochemistry Scoliosis Sarcoglycanopathies Walker-Warburg Syndrome Chromosome Mapping Calpain Chromosome Deletion Syndrome Muscle Cells DNA Mutational Analysis Muscle Contraction Base Sequence Integrin alpha Chains Biopsy Polymerase Chain Reaction Plectin Evans Blue Mice, Transgenic Oligonucleotides, Antisense Nitric Oxide Synthase Type I Fibrosis Cardiomyopathy, Dilated Oligoribonucleotides, Antisense Genetic Testing Consanguinity Connectin

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