Fuchs polymorphism gene contains trinucleotide repeat expansion. Medical search. Frequent questions

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Anatomy4

Intranuclear Inclusion Bodies Endothelium, Corneal Descemet Membrane Chromosomes, Human, X

Organisms2

Mice, Transgenic Saccharomyces cerevisiae

Diseases24

Friedreich Ataxia Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Fuchs' Endothelial Dystrophy Huntington Disease Spinocerebellar Ataxias Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Genomic Instability Frontotemporal Dementia Anticipation, Genetic Cerebellar Ataxia Chromosome Fragility Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Genetic Predisposition to Disease Amyotrophic Lateral Sclerosis Neurodegenerative Diseases Keratoconus Corneal Edema Iridocyclitis Myoclonic Epilepsies, Progressive Disease Models, Animal

Chemicals and Drugs17

Fragile X Mental Retardation Protein Iron-Binding Proteins Collagen Type VIII Nerve Tissue Proteins DNA Flap Endonucleases RNA-Binding Proteins Nuclear Proteins Genetic Markers Proteins DNA Primers Peptides Receptors, Androgen DNA-Binding Proteins RNA, Messenger MutS Homolog 2 Protein Nucleic Acid Heteroduplexes

Analytical, Diagnostic and Therapeutic Techniques and Equipment11

Pedigree Polymerase Chain Reaction Descemet Stripping Endothelial Keratoplasty Sequence Analysis, DNA Keratoplasty, Penetrating Models, Genetic Case-Control Studies DNA Mutational Analysis Chromosome Mapping Disease Models, Animal Genetic Testing

Psychiatry and Psychology2

Huntington Disease Frontotemporal Dementia

Phenomena and Processes37

Trinucleotide Repeat Expansion Trinucleotide Repeats DNA Repeat Expansion Alleles Polymorphism, Genetic Mutation Repetitive Sequences, Nucleic Acid Polymorphism, Single Nucleotide Base Sequence Microsatellite Repeats Genomic Instability Minisatellite Repeats Anticipation, Genetic Gene Frequency Tandem Repeat Sequences Nucleic Acid Conformation Inverted Repeat Sequences Genotype Chromosome Fragility Genetic Predisposition to Disease Haplotypes Phenotype Genetic Variation Genetic Markers DNA Repair Heterozygote Exons Genome, Human Genes, Dominant Transcription, Genetic Amino Acid Sequence DNA Replication Repetitive Sequences, Amino Acid Promoter Regions, Genetic Dinucleotide Repeats Genetic Linkage Chromosomes, Human, X

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care3

Age of Onset Case-Control Studies 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

Trinucleotide Repeat Expansion Trinucleotide Repeats Friedreich Ataxia DNA Repeat Expansion Spinocerebellar Degenerations Myotonic Dystrophy Fragile X Syndrome Fuchs' Endothelial Dystrophy Huntington Disease Fragile X Mental Retardation Protein Iron-Binding Proteins Alleles Polymorphism, Genetic Mutation Repetitive Sequences, Nucleic Acid Polymorphism, Single Nucleotide Collagen Type VIII Spinocerebellar Ataxias Base Sequence Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Molecular Sequence Data Nerve Tissue Proteins Microsatellite Repeats DNA Genomic Instability Pedigree Polymerase Chain Reaction Frontotemporal Dementia Flap Endonucleases Minisatellite Repeats Anticipation, Genetic Gene Frequency Tandem Repeat Sequences Nucleic Acid Conformation Inverted Repeat Sequences Age of Onset Genotype Cerebellar Ataxia Intranuclear Inclusion Bodies Chromosome Fragility Descemet Stripping Endothelial Keratoplasty Muscular Dystrophy, Oculopharyngeal Genetic Diseases, Inborn Genetic Predisposition to Disease RNA-Binding Proteins Haplotypes Phenotype Sequence Analysis, DNA Endothelium, Corneal Keratoplasty, Penetrating Amyotrophic Lateral Sclerosis Nuclear Proteins Neurodegenerative Diseases Genetic Variation Keratoconus Models, Genetic Genetic Markers DNA Repair Proteins Case-Control Studies DNA Primers Peptides Corneal Edema Heterozygote Exons Receptors, Androgen Genome, Human Mice, Transgenic Descemet Membrane Iridocyclitis Genes, Dominant DNA Mutational Analysis Transcription, Genetic DNA-Binding Proteins Chromosome Mapping Amino Acid Sequence DNA Replication Myoclonic Epilepsies, Progressive RNA, Messenger MutS Homolog 2 Protein Repetitive Sequences, Amino Acid Nucleic Acid Heteroduplexes Saccharomyces cerevisiae Promoter Regions, Genetic Dinucleotide Repeats Genetic Linkage Disease Models, Animal Genetic Testing Chromosomes, Human, X

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