Inherited diseases genetic muscular dystrophies limb girdle. Medical search. Frequent questions

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Anatomy29

Muscle, Skeletal Myoblasts Muscle Fibers, Skeletal Limb Buds Scapula Extremities Shoulder Muscles Sarcolemma Chromosomes, Human, Pair 4 X Chromosome Animal Fins Forelimb Pelvis Clavicle Cells, Cultured Diaphragm Fibroblasts Hindlimb Cell Line Satellite Cells, Skeletal Muscle Muscle Cells Myoblasts, Skeletal Lower Extremity Arm Leg Pectoralis Muscles Nuclear Envelope Sacroiliac Joint

Organisms6

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

Diseases39

Muscular Dystrophies Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Genetic Diseases, Inborn Pelvic Girdle Pain Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Muscular Diseases Distal Myopathies Muscle Weakness Fuchs' Endothelial Dystrophy Retinal Dystrophies Myositis, Inclusion Body Disease Models, Animal Neuromuscular Diseases Pelvic Pain Syndrome Neuroaxonal Dystrophies Cystic Fibrosis Sarcoglycanopathies Walker-Warburg Syndrome Genetic Predisposition to Disease Cardiomyopathies Limb Deformities, Congenital Reflex Sympathetic Dystrophy Phantom Limb Vitelliform Macular Dystrophy Myositis Brachial Plexus Neuritis Muscular Atrophy Cardiomyopathy, Dilated Myotonic Disorders Retinal Degeneration Retinitis Pigmentosa Intellectual Disability

Chemicals and Drugs40

Sarcoglycans Dystrophin Dystroglycans Caveolin 3 Muscle Proteins Calpain Connectin Utrophin Creatine Kinase Membrane Proteins Cytoskeletal Proteins Caveolins Thymopoietins Collagen Type VI Codon, Nonsense Dystrophin-Associated Proteins Laminin Lamin Type A Dystrophin-Associated Protein Complex Ferrochelatase Poly(A)-Binding Protein II DNA Genetic Markers Plectin Cystic Fibrosis Transmembrane Conductance Regulator Proteins RNA, Messenger DNA Primers Myostatin Lamins Creatine Kinase, MM Form Mannosyltransferases N-Acetylglucosaminyltransferases Membrane Glycoproteins Morpholinos Poly(A)-Binding Protein I Oxepins Integrin alpha Chains Pregnenediones Evans Blue

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Pedigree DNA Mutational Analysis Genetic Therapy Disease Models, Animal Chromosome Mapping Heterozygote Detection Biopsy Genetic Testing Immunohistochemistry Polymerase Chain Reaction Limb Salvage Muscle Strength Models, Genetic Electromyography Reverse Transcriptase Polymerase Chain Reaction Amino Acid Substitution Electroretinography Sequence Analysis, DNA Prenatal Diagnosis Cineradiography Transfection Blotting, Western Models, Molecular

Psychiatry and Psychology2

Phantom Limb Intellectual Disability

Phenomena and Processes41

Mutation Mutation, Missense Phenotype Exons Genetic Linkage Heredity Codon, Nonsense Heterozygote Base Sequence Chromosomes, Human, Pair 4 Point Mutation X Chromosome Amino Acid Sequence Genotype Genes, Recessive Alleles Genetic Predisposition to Disease Regeneration Genetic Markers Genome, Human Genetic Vectors Muscle Development Consanguinity Genes, Dominant Muscle Strength Germ-Line Mutation Gene Expression Polymorphism, Genetic Homozygote Amino Acid Substitution Sequence Homology, Amino Acid Polymorphism, Single Nucleotide Trinucleotide Repeat Expansion Glycosylation Biomechanical Phenomena Frameshift Mutation Muscle Contraction Transfection Locomotion Time Factors Gene Deletion

Disciplines and Occupations4

Immunohistochemistry Computational Biology Paleontology Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Fossils Paleontology

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care4

Age of Onset Genetic Testing Family Health Genetic Counseling

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

Muscular Dystrophies Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Sarcoglycans Dystrophin Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Genetic Diseases, Inborn Dystroglycans Pelvic Girdle Pain Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Caveolin 3 Muscle, Skeletal Muscle Proteins Calpain Pedigree Mutation Corneal Dystrophies, Hereditary Mutation, Missense Muscular Dystrophy, Oculopharyngeal Connectin Utrophin Muscular Diseases Phenotype Distal Myopathies Creatine Kinase Myoblasts Muscle Fibers, Skeletal DNA Mutational Analysis Muscle Weakness Fuchs' Endothelial Dystrophy Membrane Proteins Cytoskeletal Proteins Caveolins Exons Thymopoietins Genetic Linkage Limb Buds Retinal Dystrophies Collagen Type VI Scapula Extremities Myositis, Inclusion Body Genetic Therapy Heredity Shoulder Disease Models, Animal Codon, Nonsense Muscles Molecular Sequence Data Dystrophin-Associated Proteins Chromosome Mapping Sarcolemma Heterozygote Detection Heterozygote Age of Onset Laminin Biopsy Base Sequence Neuromuscular Diseases Genetic Testing Pelvic Pain Chromosomes, Human, Pair 4 Lamin Type A Dystrophin-Associated Protein Complex Ferrochelatase Point Mutation Syndrome Poly(A)-Binding Protein II Immunohistochemistry X Chromosome Amino Acid Sequence Animal Fins Genotype Genes, Recessive Polymerase Chain Reaction DNA Alleles Neuroaxonal Dystrophies Cystic Fibrosis Family Health Sarcoglycanopathies Walker-Warburg Syndrome Genetic Predisposition to Disease Regeneration Forelimb Limb Salvage Pelvis Cardiomyopathies Genetic Markers Clavicle Limb Deformities, Congenital Genome, Human Genetic Vectors Plectin Muscle Development Cells, Cultured Consanguinity

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