Muscular dystrophy hereditary genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy31

Muscle, Skeletal Fundus Oculi Photoreceptor Cells, Vertebrate Retina Sarcolemma Myoblasts Muscle Fibers, Skeletal Muscles Pigment Epithelium of Eye Chromosomes, Human, Pair 4 Photoreceptor Cells X Chromosome Retinal Pigment Epithelium Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Diaphragm Satellite Cells, Skeletal Muscle Myoblasts, Skeletal Muscle Cells Cornea Rod Cell Outer Segment Nuclear Envelope Descemet Membrane Cells, Cultured Myocardium Endothelium, Corneal Neuromuscular Junction Chromosomes, Human, Pair 19 Sarcomeres Facial Muscles Costameres

Organisms8

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

Diseases61

Muscular Dystrophies Retinal Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Dystrophies, Limb-Girdle Retinal Degeneration Muscular Dystrophy, Emery-Dreifuss Leber Congenital Amaurosis Retinitis Pigmentosa Fuchs' Endothelial Dystrophy Muscular Dystrophy, Oculopharyngeal Retinal Diseases Laurence-Moon Syndrome Eye Diseases, Hereditary Neuroaxonal Dystrophies Blindness Syndrome Night Blindness Bardet-Biedl Syndrome Reflex Sympathetic Dystrophy Microphthalmos Disease Models, Animal Muscular Diseases Vitelliform Macular Dystrophy Alstrom Syndrome Macular Degeneration Neuromuscular Diseases Sarcoglycanopathies Choroid Diseases Walker-Warburg Syndrome Optic Atrophy, Hereditary, Leber Usher Syndromes Cardiomyopathies Optic Atrophies, Hereditary Intellectual Disability Optic Disk Drusen Kidney Diseases, Cystic Myotonic Disorders Muscle Weakness Abnormalities, Multiple Myositis Vision Disorders Corneal Dystrophy, Juvenile Epithelial of Meesmann Cardiomyopathy, Dilated Muscular Atrophy Distal Myopathies Color Vision Defects Epidermolysis Bullosa Simplex Chromosome Deletion Fibrosis Contracture Nails, Malformed Scoliosis Disease Progression Corneal Opacity Lipodystrophy Keratoconus Myoglobinuria

Chemicals and Drugs57

Dystrophin Sarcoglycans Dystroglycans Utrophin cis-trans-Isomerases Eye Proteins Thymopoietins Collagen Type VI Peripherins Dystrophin-Associated Proteins Creatine Kinase Muscle Proteins Lamin Type A Laminin Dystrophin-Associated Protein Complex Caveolin 3 Codon, Nonsense Poly(A)-Binding Protein II Membrane Proteins Cytoskeletal Proteins Calpain Plectin Lipofuscin Connectin Intermediate Filament Proteins Nerve Tissue Proteins Rhodopsin Carrier Proteins Proteins Myostatin Lamins Collagen Type VIII Rod Opsins Membrane Glycoproteins ATP-Binding Cassette Transporters Morpholinos Creatine Kinase, MM Form Mannosyltransferases N-Acetylglucosaminyltransferases Guanylate Cyclase Poly(A)-Binding Protein I Oxepins Genetic Markers Integrin alpha Chains Pregnenediones Evans Blue DNA RNA, Messenger Caveolins Cardiotoxins Extracellular Matrix Proteins Oligoribonucleotides, Antisense Nitric Oxide Synthase Type I Glycosyltransferases DNA Probes Oligonucleotides, Antisense MyoD Protein

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

Electroretinography Pedigree DNA Mutational Analysis Heterozygote Detection Visual Acuity Disease Models, Animal Chromosome Mapping Fluorescein Angiography Genetic Testing Polymerase Chain Reaction Genetic Therapy Tomography, Optical Coherence Heteroduplex Analysis Muscle Strength Visual Field Tests Ophthalmoscopy Immunohistochemistry Keratoplasty, Penetrating Biopsy Prenatal Diagnosis Blotting, Western Sequence Analysis, DNA Amino Acid Substitution Fluorescent Antibody Technique Electrooculography Reverse Transcriptase Polymerase Chain Reaction Electromyography

Psychiatry and Psychology4

Visual Acuity Intellectual Disability Visual Fields Vision, Ocular

Phenomena and Processes49

Consanguinity Genes, Recessive Mutation Exons Phenotype Genes, Dominant Genetic Linkage Mutation, Missense Chromosomes, Human, Pair 4 Visual Acuity Codon, Nonsense Dark Adaptation Heterozygote X Chromosome Homozygote Base Sequence Frameshift Mutation Lod Score Polymorphism, Single-Stranded Conformational Haplotypes Exome Visual Fields Muscle Development Regeneration Trinucleotide Repeat Expansion Genotype Amino Acid Sequence Muscle Strength Point Mutation Glycosylation Genetic Markers Gene Deletion Muscle Contraction Gene Expression Regulation Sequence Deletion Amino Acid Substitution Vision, Ocular Chromosome Deletion Genetic Vectors Alternative Splicing Alleles Tandem Repeat Sequences Transgenes Founder Effect Fluorescence Chromosomes, Human, Pair 19 Light Mosaicism Gene Expression

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care4

Age of Onset Genetic Testing Genetic Counseling Family Health

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

Muscular Dystrophies Retinal Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Dystrophin Muscular Dystrophy, Facioscapulohumeral Corneal Dystrophies, Hereditary Muscular Dystrophies, Limb-Girdle Retinal Degeneration Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Leber Congenital Amaurosis Retinitis Pigmentosa Fuchs' Endothelial Dystrophy Dystroglycans Muscular Dystrophy, Oculopharyngeal Electroretinography Pedigree Utrophin cis-trans-Isomerases Muscle, Skeletal Fundus Oculi Eye Proteins Consanguinity Genes, Recessive Mutation Thymopoietins Retinal Diseases DNA Mutational Analysis Laurence-Moon Syndrome Collagen Type VI Exons Phenotype Photoreceptor Cells, Vertebrate Eye Diseases, Hereditary Retina Peripherins Neuroaxonal Dystrophies Blindness Dystrophin-Associated Proteins Heterozygote Detection Sarcolemma Genes, Dominant Creatine Kinase Myoblasts Muscle Proteins Genetic Linkage Muscle Fibers, Skeletal Muscles Pigment Epithelium of Eye Syndrome Mutation, Missense Night Blindness Chromosomes, Human, Pair 4 Lamin Type A Bardet-Biedl Syndrome Reflex Sympathetic Dystrophy Visual Acuity Laminin Photoreceptor Cells Dystrophin-Associated Protein Complex Microphthalmos Caveolin 3 Disease Models, Animal Codon, Nonsense Poly(A)-Binding Protein II Dark Adaptation Molecular Sequence Data Chromosome Mapping Muscular Diseases Heterozygote X Chromosome Fluorescein Angiography Vitelliform Macular Dystrophy Alstrom Syndrome Retinal Pigment Epithelium Macular Degeneration Membrane Proteins Neuromuscular Diseases Homozygote Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Cytoskeletal Proteins Base Sequence Frameshift Mutation Age of Onset Sarcoglycanopathies Choroid Diseases Walker-Warburg Syndrome Calpain Optic Atrophy, Hereditary, Leber Usher Syndromes Cardiomyopathies Genetic Testing Optic Atrophies, Hereditary Intellectual Disability Lod Score Polymorphism, Single-Stranded Conformational

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