Fecd cases homozygous for repeat expansion. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy15

Endothelium, Corneal Descemet Membrane Intranuclear Inclusion Bodies Chromosomes, Human, Pair 9 Cornea Inclusion Bodies Brain Cells, Cultured Cell Line Neurons Cell Nucleus HeLa Cells Cerebellum Fibroblasts Muscle, Skeletal

Organisms3

Mice, Transgenic Mice, Inbred C57BL Saccharomyces cerevisiae

Diseases30

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

Chemicals and Drugs27

Collagen Type VIII Fragile X Mental Retardation Protein Iron-Binding Proteins Nerve Tissue Proteins Proteins Flap Endonucleases DNA Cystatin B RNA-Binding Proteins Basic Helix-Loop-Helix Leucine Zipper Transcription Factors Nuclear Proteins Peptides tert-Butylhydroperoxide DNA Polymerase beta Transcription Factors DNA-Binding Proteins DNA Primers RNA, Messenger Genetic Markers TATA-Box Binding Protein MutS Homolog 2 Protein Protein-Serine-Threonine Kinases RNA Receptors, Androgen Repressor Proteins tau Proteins Saccharomyces cerevisiae Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Corneal Pachymetry Corneal Transplantation Pedigree Polymerase Chain Reaction Sequence Analysis, DNA Palatal Expansion Technique Disease Models, Animal Gene Knock-In Techniques Real-Time Polymerase Chain Reaction Models, Genetic DNA Mutational Analysis Autopsy Neuroimaging Microscopy, Confocal Genetic Testing Tissue Expansion Cohort Studies Cloning, Molecular Models, Biological Reverse Transcriptase Polymerase Chain Reaction Sequence Alignment Immunohistochemistry

Psychiatry and Psychology4

Frontotemporal Dementia Huntington Disease Frontotemporal Lobar Degeneration Neuropsychological Tests

Phenomena and Processes54

DNA Repeat Expansion Trinucleotide Repeat Expansion Trinucleotide Repeats Repetitive Sequences, Nucleic Acid Tandem Repeat Sequences Alleles Base Sequence Minisatellite Repeats Repetitive Sequences, Amino Acid Inverted Repeat Sequences Anticipation, Genetic Mutation Microsatellite Repeats Genomic Instability Genotype Phenotype Chromosomes, Human, Pair 9 Ankyrin Repeat Chromosome Fragility Dinucleotide Repeats Amino Acid Sequence Genes, Dominant Nucleic Acid Conformation Haplotypes Founder Effect Polymorphism, Genetic Mosaicism Heterozygote Exons Genetic Variation Chromosome Fragile Sites Genetic Markers Introns Evolution, Molecular DNA Mismatch Repair Transcription, Genetic Genome, Human DNA Repair Genetic Predisposition to Disease DNA Replication Gene Expression Regulation Recombination, Genetic Promoter Regions, Genetic Gene Frequency Genetic Linkage Protein Binding Gene Expression Phylogeny DNA Methylation Oxidative Stress HIV Long Terminal Repeat Alternative Splicing Cell Proliferation Polymorphism, Single Nucleotide

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Health Care4

Age of Onset Tissue Banks Genetic Testing Cohort Studies

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

DNA Repeat Expansion Fuchs' Endothelial Dystrophy Trinucleotide Repeat Expansion Collagen Type VIII Trinucleotide Repeats Myotonic Dystrophy Friedreich Ataxia Frontotemporal Dementia Spinocerebellar Degenerations Endothelium, Corneal Spinocerebellar Ataxias Fragile X Syndrome Huntington Disease Fragile X Mental Retardation Protein Repetitive Sequences, Nucleic Acid Amyotrophic Lateral Sclerosis Tandem Repeat Sequences Corneal Pachymetry Corneal Edema Machado-Joseph Disease Iron-Binding Proteins Heredodegenerative Disorders, Nervous System Nerve Tissue Proteins Myoclonic Epilepsies, Progressive Alleles Base Sequence Minisatellite Repeats Repetitive Sequences, Amino Acid Molecular Sequence Data Corneal Transplantation Inverted Repeat Sequences Anticipation, Genetic Pedigree Descemet Membrane Age of Onset Mutation Proteins Flap Endonucleases Microsatellite Repeats Cerebellar Ataxia Unverricht-Lundborg Syndrome Myotonic Disorders Intranuclear Inclusion Bodies Muscular Dystrophy, Oculopharyngeal DNA Genomic Instability Cystatin B Genotype Phenotype Frontotemporal Lobar Degeneration Chromosomes, Human, Pair 9 Ataxia RNA-Binding Proteins Basic Helix-Loop-Helix Leucine Zipper Transcription Factors Polymerase Chain Reaction Ankyrin Repeat Cornea Nuclear Proteins Peptides Mice, Transgenic tert-Butylhydroperoxide Chromosome Fragility Genetic Diseases, Inborn Dinucleotide Repeats Amino Acid Sequence Genes, Dominant Nucleic Acid Conformation DNA Polymerase beta Transcription Factors Sequence Analysis, DNA DNA-Binding Proteins Haplotypes Palatal Expansion Technique Neurodegenerative Diseases Tissue Banks Disease Models, Animal Founder Effect Gene Knock-In Techniques Polymorphism, Genetic Real-Time Polymerase Chain Reaction Inclusion Bodies DNA Primers Mosaicism RNA, Messenger Brain Heterozygote Models, Genetic Exons Genetic Variation Chromosome Fragile Sites Tremor Cells, Cultured Genetic Markers TATA-Box Binding Protein Cell Line Introns Evolution, Molecular DNA Mutational Analysis DNA Mismatch Repair Transcription, Genetic

No FAQ available that match "fecd cases homozygous for repeat expansion"