Muscular dystrophy myotonic dystrophy. Medical search. Frequent questions

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Anatomy10

Muscle, Skeletal Myoblasts Muscles Muscle Fibers, Skeletal Chromosomes, Human, Pair 19 Sarcolemma Chromosomes, Human, Pair 4 X Chromosome Myoblasts, Skeletal Chromosomes, Human, 19-20

Organisms2

Mice, Inbred mdx Mice, Transgenic

Diseases27

Myotonic Dystrophy Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Dystrophies, Limb-Girdle Myotonic Disorders Muscular Dystrophy, Emery-Dreifuss Fuchs' Endothelial Dystrophy Muscular Dystrophy, Oculopharyngeal Retinal Dystrophies Myotonia Neuroaxonal Dystrophies Neuromuscular Diseases Muscular Diseases Muscle Weakness Disease Models, Animal Reflex Sympathetic Dystrophy Myotonia Congenita Vitelliform Macular Dystrophy Lens Diseases Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Retinal Degeneration Retinitis Pigmentosa

Chemicals and Drugs26

Dystrophin Sarcoglycans Dystroglycans Utrophin Thymopoietins RNA-Binding Proteins Dystrophin-Associated Proteins Collagen Type VI Protein-Serine-Threonine Kinases Creatine Kinase Muscle Proteins Lamin Type A Laminin Dystrophin-Associated Protein Complex Caveolin 3 Poly(A)-Binding Protein II Cytoskeletal Proteins Calpain RNA DNA RNA, Messenger Plectin Genetic Markers 3' Untranslated Regions Connectin Membrane Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Pedigree Heterozygote Detection Disease Models, Animal DNA Mutational Analysis Polymerase Chain Reaction Chromosome Mapping Prenatal Diagnosis Genetic Testing Electroretinography Electromyography Genetic Therapy Blotting, Southern Biopsy

Phenomena and Processes25

Trinucleotide Repeat Expansion Trinucleotide Repeats Mutation Exons Chromosomes, Human, Pair 19 DNA Repeat Expansion Phenotype Genetic Linkage Alternative Splicing Base Sequence Repetitive Sequences, Nucleic Acid Chromosomes, Human, Pair 4 X Chromosome Genes, Dominant Genes, Recessive Alleles Heterozygote RNA Splicing Consanguinity Chromosomes, Human, 19-20 Founder Effect Genetic Markers 3' Untranslated Regions Muscle Development Regeneration

Disciplines and Occupations1

Genetic Counseling

Information Science2

Base Sequence Molecular Sequence Data

Health Care3

Age of Onset Genetic Testing Genetic Counseling

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

Myotonic Dystrophy Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Dystrophies, Limb-Girdle Myotonic Disorders Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Trinucleotide Repeat Expansion Sarcoglycans Muscle, Skeletal Fuchs' Endothelial Dystrophy Dystroglycans Muscular Dystrophy, Oculopharyngeal Utrophin Trinucleotide Repeats Retinal Dystrophies Pedigree Myotonia Myoblasts Thymopoietins RNA-Binding Proteins Dystrophin-Associated Proteins Muscles Collagen Type VI Mutation Heterozygote Detection Exons Muscle Fibers, Skeletal Chromosomes, Human, Pair 19 Protein-Serine-Threonine Kinases DNA Repeat Expansion Neuroaxonal Dystrophies Neuromuscular Diseases Sarcolemma Phenotype Creatine Kinase Muscular Diseases Muscle Proteins Genetic Linkage Alternative Splicing Base Sequence Repetitive Sequences, Nucleic Acid Muscle Weakness Chromosomes, Human, Pair 4 Disease Models, Animal Lamin Type A Molecular Sequence Data Reflex Sympathetic Dystrophy Laminin Dystrophin-Associated Protein Complex Caveolin 3 Myotonia Congenita Poly(A)-Binding Protein II X Chromosome Vitelliform Macular Dystrophy DNA Mutational Analysis Genes, Dominant Cytoskeletal Proteins Genes, Recessive Mice, Transgenic Polymerase Chain Reaction Lens Diseases Chromosome Mapping Alleles Heterozygote Sarcoglycanopathies Walker-Warburg Syndrome Calpain RNA RNA Splicing Consanguinity Myoblasts, Skeletal Cardiomyopathies Age of Onset Chromosomes, Human, 19-20 DNA Prenatal Diagnosis RNA, Messenger Genetic Testing Founder Effect Retinal Degeneration Plectin Electroretinography Genetic Markers 3' Untranslated Regions Electromyography Genetic Therapy Muscle Development Blotting, Southern Regeneration Retinitis Pigmentosa Connectin Genetic Counseling Membrane Proteins Biopsy

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