Becker muscular dystrophy. Medical search. Frequent questions

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Anatomy8

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

Organisms4

Mice, Inbred mdx Nepeta Viola Mice, Inbred C57BL

Diseases26

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Cardiomyopathy, Dilated Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Chromosome Deletion Cardiomyopathies Fuchs' Endothelial Dystrophy Retinal Dystrophies Muscular Diseases Myotonia Congenita Neuromuscular Diseases Neuroaxonal Dystrophies Disease Models, Animal Sarcoglycanopathies Walker-Warburg Syndrome Reflex Sympathetic Dystrophy Muscle Weakness Vitelliform Macular Dystrophy Melanosis Myositis

Chemicals and Drugs26

Dystrophin Utrophin Sarcoglycans Deoxyribonuclease HindIII Dystroglycans Creatine Kinase Muscle Proteins DNA Probes Cytoskeletal Proteins Thymopoietins Collagen Type VI DNA Dystrophin-Associated Proteins Lamin Type A Dystrophin-Associated Protein Complex Laminin Caveolin 3 Poly(A)-Binding Protein II Calpain Oligoribonucleotides, Antisense Codon, Nonsense Plectin Connectin Membrane Proteins Myostatin Lamins

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

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

Phenomena and Processes21

Exons X Chromosome Genetic Linkage Phenotype Heterozygote Gene Deletion Chromosome Deletion Frameshift Mutation Mutation Sequence Deletion Base Sequence RNA Splicing Point Mutation Chromosomes, Human, Pair 4 Codon, Nonsense Genes, Recessive Consanguinity Muscle Development Regeneration Muscle Strength Genes, Dominant

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science2

Molecular Sequence Data Base Sequence

Health Care2

Genetic Testing Genetic Counseling

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Dystrophin Muscular Dystrophy, Animal Heterozygote Detection Utrophin Sarcoglycans Mice, Inbred mdx Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Exons Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Deoxyribonuclease HindIII Pedigree X Chromosome Muscle, Skeletal Cardiomyopathy, Dilated Blood Stains Corneal Dystrophies, Hereditary Dystroglycans Sarcolemma Muscular Dystrophy, Oculopharyngeal Prenatal Diagnosis Creatine Kinase Genetic Linkage Muscles Phenotype Heterozygote Gene Deletion Chromosome Deletion Frameshift Mutation Mutation Cardiomyopathies Polymerase Chain Reaction Muscle Proteins DNA Probes Sequence Deletion Cytoskeletal Proteins Fuchs' Endothelial Dystrophy Molecular Sequence Data Thymopoietins Genetic Testing DNA Mutational Analysis Retinal Dystrophies Collagen Type VI Base Sequence RNA Splicing DNA Dystrophin-Associated Proteins Point Mutation Blotting, Southern Myoblasts Immunohistochemistry Muscle Fibers, Skeletal Chromosomes, Human, Pair 4 Lamin Type A Dystrophin-Associated Protein Complex Laminin Caveolin 3 Poly(A)-Binding Protein II Muscular Diseases Myotonia Congenita Nepeta Neuromuscular Diseases Echocardiography Neuroaxonal Dystrophies Disease Models, Animal Sarcoglycanopathies Walker-Warburg Syndrome Calpain Genetic Counseling Oligoribonucleotides, Antisense Codon, Nonsense Genes, Recessive Plectin Chromosome Mapping Viola Genetic Therapy Consanguinity Connectin Muscle Development Regeneration Biopsy Reflex Sympathetic Dystrophy Membrane Proteins Muscle Weakness Diaphragm Muscle Strength Vitelliform Macular Dystrophy Melanosis Myositis Myostatin Mice, Inbred C57BL Genes, Dominant Lamins

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