Congenital muscular dy muscular dystrophies. Medical search. Frequent questions

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Anatomy19

Muscle, Skeletal Sarcolemma Muscle Fibers, Skeletal Muscles Myoblasts Chromosomes, Human, Pair 4 X Chromosome Diaphragm Satellite Cells, Skeletal Muscle Muscle Cells Myoblasts, Skeletal Nuclear Envelope Cells, Cultured Basement Membrane Myocardium Neuromuscular Junction Fundus Oculi Sarcomeres Costameres

Organisms7

Mice, Inbred mdx Mice, Inbred C57BL Dependovirus Mice, Mutant Strains Mice, Transgenic Mice, Knockout Dogs

Diseases39

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Retinal Dystrophies Muscular Diseases Neuromuscular Diseases Disease Models, Animal Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Reflex Sympathetic Dystrophy Muscle Weakness Vitelliform Macular Dystrophy Myositis Cardiomyopathy, Dilated Muscular Atrophy Myotonic Disorders Syndrome Retinal Degeneration Retinitis Pigmentosa Distal Myopathies Intellectual Disability Fibrosis Epidermolysis Bullosa Simplex Chromosome Deletion Contracture Scoliosis Corneal Dystrophy, Juvenile Epithelial of Meesmann Myoglobinuria Disease Progression Lipodystrophy

Chemicals and Drugs45

Dystrophin Sarcoglycans Dystroglycans Utrophin Thymopoietins Collagen Type VI Laminin Dystrophin-Associated Proteins Muscle Proteins Creatine Kinase Lamin Type A Dystrophin-Associated Protein Complex Caveolin 3 Poly(A)-Binding Protein II Dysprosium Oxepins Cytoskeletal Proteins Calpain Plectin Connectin Membrane Proteins Myostatin Lamins Creatine Kinase, MM Form Mannosyltransferases N-Acetylglucosaminyltransferases Poly(A)-Binding Protein I Membrane Glycoproteins Morpholinos Integrin alpha Chains Codon, Nonsense Pregnenediones Evans Blue Genetic Markers Caveolins RNA, Messenger Cardiotoxins DNA Lanthanoid Series Elements Nitric Oxide Synthase Type I Glycosyltransferases Oligoribonucleotides, Antisense Collagen Type VIII Glycerol Kinase Oligonucleotides, Antisense

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

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

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes37

Chromosomes, Human, Pair 4 Exons Mutation X Chromosome Phenotype Genetic Linkage Genes, Recessive Muscle Strength Consanguinity Muscle Development Regeneration Heterozygote Genes, Dominant Base Sequence Mutation, Missense Trinucleotide Repeat Expansion Homozygote Glycosylation Frameshift Mutation Codon, Nonsense Amino Acid Sequence Gene Deletion Genetic Markers Gene Expression Regulation Muscle Contraction Sequence Deletion Point Mutation Chromosome Deletion Genetic Vectors Genotype Tandem Repeat Sequences Lod Score Transgenes Haplotypes Gene Expression Founder Effect Alleles

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Genetic Counseling Genetic Testing Age of Onset

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Corneal Dystrophies, Hereditary Dystroglycans Muscular Dystrophy, Oculopharyngeal Utrophin Muscle, Skeletal Fuchs' Endothelial Dystrophy Thymopoietins Retinal Dystrophies Collagen Type VI Pedigree Laminin Dystrophin-Associated Proteins Sarcolemma Heterozygote Detection Muscle Proteins Muscle Fibers, Skeletal Creatine Kinase Muscles Myoblasts Chromosomes, Human, Pair 4 Lamin Type A Dystrophin-Associated Protein Complex Exons Caveolin 3 Mutation Poly(A)-Binding Protein II Dysprosium Muscular Diseases X Chromosome Phenotype Oxepins Neuromuscular Diseases Disease Models, Animal Cytoskeletal Proteins Neuroaxonal Dystrophies Genetic Linkage Sarcoglycanopathies Walker-Warburg Syndrome Calpain Cardiomyopathies Genes, Recessive Plectin Diaphragm Muscle Strength Genetic Therapy Consanguinity Connectin Muscle Development Regeneration Reflex Sympathetic Dystrophy Membrane Proteins Muscle Weakness DNA Mutational Analysis Molecular Sequence Data Mice, Inbred C57BL Vitelliform Macular Dystrophy Heterozygote Chromosome Mapping Myositis Myostatin Genes, Dominant Lamins Satellite Cells, Skeletal Muscle Dependovirus Base Sequence Mice, Mutant Strains Mice, Transgenic Immunohistochemistry Mutation, Missense Cardiomyopathy, Dilated Electroretinography Muscular Atrophy Trinucleotide Repeat Expansion Mice, Knockout Muscle Cells Myotonic Disorders Homozygote Glycosylation Myoblasts, Skeletal Polymerase Chain Reaction Creatine Kinase, MM Form Mannosyltransferases Biopsy N-Acetylglucosaminyltransferases Prenatal Diagnosis Syndrome Retinal Degeneration Poly(A)-Binding Protein I Membrane Glycoproteins Morpholinos

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