Subtypes genetic autosomal recessive form muscular dystrophies. Medical search. Frequent questions

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Anatomy28

Muscle, Skeletal X Chromosome Sarcolemma Chromosomes, Human, Pair 4 Muscles Myoblasts Muscle Fibers, Skeletal Chromosomes, Human, Pair 2 Diaphragm Fundus Oculi Cells, Cultured Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 19 Mitochondria Cell Line Satellite Cells, Skeletal Muscle Fibroblasts Chromosomes, Human, Pair 5 Muscle Cells Myoblasts, Skeletal Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 10 Photoreceptor Cells, Vertebrate Brain Myocardium Nuclear Envelope Retina Skin

Organisms8

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

Diseases90

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Granulomatous Disease, Chronic Muscular Dystrophy, Facioscapulohumeral Spastic Paraplegia, Hereditary Syndrome Muscular Dystrophy, Emery-Dreifuss Immunologic Deficiency Syndromes Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Parkinson Disease Arthrogryposis Dysostoses Abnormalities, Multiple Fuchs' Endothelial Dystrophy Retinal Dystrophies Polycystic Kidney, Autosomal Recessive Hearing Loss, Sensorineural Ectodermal Dysplasia Deafness Retinitis Pigmentosa Charcot-Marie-Tooth Disease Osteogenesis Imperfecta Muscular Diseases Disease Models, Animal Intellectual Disability Neuromuscular Diseases Neuroaxonal Dystrophies Microcephaly Walker-Warburg Syndrome Hypotrichosis Ichthyosis Cardiomyopathies Retinal Degeneration Vitelliform Macular Dystrophy Sarcoglycanopathies Ichthyosiform Erythroderma, Congenital Muscle Weakness Eye Diseases, Hereditary Nails, Malformed Chromosome Disorders Reflex Sympathetic Dystrophy Ichthyosis, Lamellar Dwarfism Cerebellar Ataxia Eye Abnormalities Muscular Atrophy Osteochondrodysplasias Myositis Myotonic Disorders Cardiomyopathy, Dilated Genetic Diseases, Inborn Muscular Atrophy, Spinal Bone Diseases, Developmental Distal Myopathies Osteopetrosis Epidermolysis Bullosa Myotonia Congenita Metabolism, Inborn Errors Albinism, Oculocutaneous Genetic Predisposition to Disease Chromosome Deletion Contracture Night Blindness Genetic Diseases, X-Linked Microphthalmos Foot Deformities, Congenital Muscle Hypotonia Disease Progression Color Vision Defects Kidney Diseases, Cystic Macular Degeneration Friedreich Ataxia Hair Diseases Cutis Laxa Leber Congenital Amaurosis Cystinosis Retinal Diseases Lipodystrophy Hearing Loss Rare Diseases Epidermolysis Bullosa Simplex Amino Acid Metabolism, Inborn Errors Optic Atrophy Keratoderma, Palmoplantar Tooth Abnormalities Syndactyly

Chemicals and Drugs48

Dystrophin Sarcoglycans Dystroglycans Genetic Markers Utrophin Codon, Nonsense Thymopoietins Collagen Type VI Collagen Type XI Muscle Proteins Dystrophin-Associated Proteins Creatine Kinase Lamin Type A Laminin Dystrophin-Associated Protein Complex Caveolin 3 Cytoskeletal Proteins Membrane Proteins Poly(A)-Binding Protein II Ubiquitin-Protein Ligases Calpain Plectin Eye Proteins Connectin RNA, Messenger DNA Membrane Glycoproteins DNA Primers Myostatin Lamins Mannosyltransferases N-Acetylglucosaminyltransferases Proteins Nerve Tissue Proteins Creatine Kinase, MM Form RNA Splice Sites Morpholinos Poly(A)-Binding Protein I Nuclear Proteins Oxepins Carrier Proteins Extracellular Matrix Proteins Integrin alpha Chains Codon, Terminator Evans Blue Pregnenediones Survival of Motor Neuron 1 Protein DNA, Complementary

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Pedigree DNA Mutational Analysis Chromosome Mapping Heterozygote Detection Disease Models, Animal Polymerase Chain Reaction Electroretinography Genetic Testing Genetic Therapy Immunohistochemistry Prenatal Diagnosis Sequence Analysis, DNA Muscle Strength Blotting, Western Biopsy Reverse Transcriptase Polymerase Chain Reaction Crosses, Genetic Fluorescent Antibody Technique Models, Genetic Amino Acid Substitution Blotting, Southern Cloning, Molecular Magnetic Resonance Imaging

Psychiatry and Psychology3

Intellectual Disability Family Siblings

Phenomena and Processes60

Genes, Recessive Consanguinity Mutation Genetic Linkage Homozygote Mutation, Missense Lod Score Exons Phenotype Heterozygote Haplotypes Base Sequence Genetic Markers Amino Acid Sequence Genes, Dominant Codon, Nonsense X Chromosome Genotype Chromosomes, Human, Pair 4 Microsatellite Repeats Frameshift Mutation Alleles Founder Effect Point Mutation Polymorphism, Single-Stranded Conformational Genetic Heterogeneity Sequence Deletion Chromosomes, Human, Pair 2 Gene Deletion Regeneration Muscle Development Exome Muscle Strength Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 19 Glycosylation Polymorphism, Genetic Introns Chromosomes, Human, Pair 5 Gene Expression Regulation Gene Expression Sequence Homology, Amino Acid Trinucleotide Repeat Expansion Genetic Predisposition to Disease Chromosome Deletion Alternative Splicing Polymorphism, Restriction Fragment Length RNA Splice Sites Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 10 Protein Structure, Tertiary RNA Splicing Codon, Terminator Muscle Contraction Genetic Vectors Amino Acid Substitution Mosaicism Gene Frequency Polymorphism, Single Nucleotide Time Factors

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Family Siblings

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups4

Infant, Newborn Arabs Siblings Jews

Health Care4

Family Health Genetic Testing Age of Onset Genetic Counseling

Geographicals2

Pakistan Tunisia

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 Named Groups Health Care Geographicals

Genes, Recessive Muscular Dystrophies Muscular Dystrophy, Duchenne Pedigree Muscular Dystrophy, Animal Consanguinity Dystrophin Mutation Genetic Linkage Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Granulomatous Disease, Chronic DNA Mutational Analysis Homozygote Muscular Dystrophy, Facioscapulohumeral Spastic Paraplegia, Hereditary Chromosome Mapping Mutation, Missense Lod Score Mice, Inbred mdx Syndrome Muscular Dystrophy, Emery-Dreifuss Exons Sarcoglycans Phenotype Heterozygote Immunologic Deficiency Syndromes Corneal Dystrophies, Hereditary Haplotypes Molecular Sequence Data Dystroglycans Base Sequence Muscular Dystrophy, Oculopharyngeal Genetic Markers Utrophin Muscle, Skeletal Amino Acid Sequence Genes, Dominant Parkinson Disease Arthrogryposis Dysostoses Abnormalities, Multiple Codon, Nonsense X Chromosome Fuchs' Endothelial Dystrophy Retinal Dystrophies Heterozygote Detection Polycystic Kidney, Autosomal Recessive Thymopoietins Collagen Type VI Hearing Loss, Sensorineural Ectodermal Dysplasia Genotype Deafness Collagen Type XI Retinitis Pigmentosa Charcot-Marie-Tooth Disease Family Health Sarcolemma Chromosomes, Human, Pair 4 Muscle Proteins Dystrophin-Associated Proteins Osteogenesis Imperfecta Creatine Kinase Muscular Diseases Microsatellite Repeats Muscles Myoblasts Muscle Fibers, Skeletal Lamin Type A Laminin Disease Models, Animal Frameshift Mutation Intellectual Disability Dystrophin-Associated Protein Complex Caveolin 3 Cytoskeletal Proteins Membrane Proteins Neuromuscular Diseases Neuroaxonal Dystrophies Poly(A)-Binding Protein II Ubiquitin-Protein Ligases Microcephaly Walker-Warburg Syndrome Alleles Hypotrichosis Polymerase Chain Reaction Electroretinography Infant, Newborn Genetic Testing Founder Effect Ichthyosis Cardiomyopathies Calpain Retinal Degeneration Vitelliform Macular Dystrophy Point Mutation Sarcoglycanopathies Age of Onset Genetic Therapy

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