Examination dystrophy genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy18

X Chromosome Muscles Fundus Oculi Photoreceptor Cells, Vertebrate Retina Pigment Epithelium of Eye Photoreceptor Cells Retinal Pigment Epithelium Muscle, Skeletal Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Myoblasts Cornea Sarcolemma Chromosomes, Human, Pair 4 Muscle Fibers, Skeletal Rod Cell Outer Segment Descemet Membrane

Organisms3

Mice, Inbred mdx Rats, Mutant Strains Mice, Inbred C57BL

Diseases40

Retinal Dystrophies Muscular Dystrophies Myotonic Dystrophy Muscular Dystrophy, Duchenne Corneal Dystrophies, Hereditary Retinal Degeneration Muscular Dystrophy, Animal Leber Congenital Amaurosis Retinitis Pigmentosa Fuchs' Endothelial Dystrophy Muscular Dystrophy, Facioscapulohumeral Retinal Diseases Muscular Dystrophy, Emery-Dreifuss Laurence-Moon Syndrome Eye Diseases, Hereditary Neuroaxonal Dystrophies Blindness Night Blindness Bardet-Biedl Syndrome Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Microphthalmos Vitelliform Macular Dystrophy Macular Degeneration Alstrom Syndrome Syndrome Choroid Diseases Optic Atrophy, Hereditary, Leber Usher Syndromes Optic Atrophies, Hereditary Optic Disk Drusen Kidney Diseases, Cystic Vision Disorders Disease Models, Animal Myotonic Disorders Abnormalities, Multiple Intellectual Disability Corneal Dystrophy, Juvenile Epithelial of Meesmann Color Vision Defects Muscular Diseases

Chemicals and Drugs26

Dystrophin cis-trans-Isomerases Eye Proteins Peripherins Sarcoglycans Dystroglycans Utrophin Codon, Nonsense Lipofuscin Rhodopsin Thymopoietins Membrane Proteins Intermediate Filament Proteins Collagen Type VI Nerve Tissue Proteins Collagen Type VIII Carrier Proteins Dystrophin-Associated Proteins Proteins Rod Opsins Creatine Kinase ATP-Binding Cassette Transporters Guanylate Cyclase Muscle Proteins Lamin Type A Laminin

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Chromosome Mapping Tomography, Optical Coherence Physical Examination Heteroduplex Analysis Ophthalmoscopy Visual Field Tests Disease Models, Animal Genetic Testing Polymerase Chain Reaction Heterozygote Detection Keratoplasty, Penetrating

Psychiatry and Psychology3

Visual Acuity Visual Fields Intellectual Disability

Phenomena and Processes26

X Chromosome Consanguinity Genes, Recessive Mutation Visual Acuity Phenotype Genes, Dominant Dark Adaptation Exons Mutation, Missense Genetic Linkage Codon, Nonsense Visual Fields Heterozygote Homozygote Base Sequence Frameshift Mutation Lod Score Exome Polymorphism, Single-Stranded Conformational Haplotypes Trinucleotide Repeat Expansion Genotype Amino Acid Sequence Chromosomes, Human, Pair 4 Point Mutation

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care2

Age of Onset Genetic Testing

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

Retinal Dystrophies Muscular Dystrophies Dystrophin Myotonic Dystrophy Muscular Dystrophy, Duchenne Corneal Dystrophies, Hereditary Retinal Degeneration Muscular Dystrophy, Animal Leber Congenital Amaurosis X Chromosome Retinitis Pigmentosa Fuchs' Endothelial Dystrophy Electroretinography Muscles cis-trans-Isomerases Muscular Dystrophy, Facioscapulohumeral Fundus Oculi Eye Proteins Pedigree Consanguinity Genes, Recessive Retinal Diseases Muscular Dystrophy, Emery-Dreifuss Mice, Inbred mdx Laurence-Moon Syndrome Photoreceptor Cells, Vertebrate Eye Diseases, Hereditary Mutation Retina Peripherins Neuroaxonal Dystrophies DNA Mutational Analysis Blindness Sarcoglycans Pigment Epithelium of Eye Night Blindness Visual Acuity Phenotype Bardet-Biedl Syndrome Muscular Dystrophy, Oculopharyngeal Genes, Dominant Dystroglycans Reflex Sympathetic Dystrophy Photoreceptor Cells Microphthalmos Dark Adaptation Fluorescein Angiography Vitelliform Macular Dystrophy Macular Degeneration Utrophin Retinal Pigment Epithelium Alstrom Syndrome Exons Muscle, Skeletal Syndrome Mutation, Missense Retinal Cone Photoreceptor Cells Retinal Rod Photoreceptor Cells Choroid Diseases Genetic Linkage Codon, Nonsense Optic Atrophy, Hereditary, Leber Usher Syndromes Optic Atrophies, Hereditary Molecular Sequence Data Visual Fields Chromosome Mapping Lipofuscin Optic Disk Drusen Kidney Diseases, Cystic Heterozygote Rats, Mutant Strains Tomography, Optical Coherence Homozygote Age of Onset Base Sequence Physical Examination Heteroduplex Analysis Ophthalmoscopy Frameshift Mutation Lod Score Visual Field Tests Exome Rhodopsin Thymopoietins Polymorphism, Single-Stranded Conformational Vision Disorders Disease Models, Animal Myotonic Disorders Abnormalities, Multiple Haplotypes Genetic Testing Membrane Proteins Trinucleotide Repeat Expansion Intermediate Filament Proteins Collagen Type VI Nerve Tissue Proteins Intellectual Disability Polymerase Chain Reaction Corneal Dystrophy, Juvenile Epithelial of Meesmann

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