Fragile x syndrome and myotonic dystrophy. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy10

X Chromosome Dendritic Spines Chromosomes, Human, Pair 19 Muscle, Skeletal Brain Synapses Dendrites Chromosomes, Human, X Neurons Myoblasts

Organisms2

Mice, Knockout Mice, Inbred C57BL

Diseases27

Fragile X Syndrome Myotonic Dystrophy Muscular Dystrophies Syndrome Myotonic Disorders Sex Chromosome Aberrations Muscular Dystrophy, Duchenne Intellectual Disability Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Myotonia Down Syndrome Muscular Dystrophy, Facioscapulohumeral Disease Models, Animal Chromosome Fragility Fuchs' Endothelial Dystrophy Epilepsy, Reflex Ataxia Tremor Language Development Disorders Retinal Dystrophies Communication Disorders Language Disorders Primary Ovarian Insufficiency Metabolic Syndrome X Myotonia Congenita Muscular Dystrophy, Emery-Dreifuss

Chemicals and Drugs14

Fragile X Mental Retardation Protein RNA-Binding Proteins Nerve Tissue Proteins Receptors, Metabotropic Glutamate Receptor, Metabotropic Glutamate 5 Methoxyhydroxyphenylglycol Protein-Serine-Threonine Kinases DNA Lithium Compounds Dystrophin RNA, Messenger RNA DNA Probes Genetic Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Heterozygote Detection Pedigree Genetic Testing Disease Models, Animal Blotting, Southern Prenatal Diagnosis Polymerase Chain Reaction DNA Mutational Analysis Narration

Psychiatry and Psychology14

Intellectual Disability Autistic Disorder Nonverbal Communication Child Development Disorders, Pervasive Intelligence Tests Intelligence Child Language Communication Disorders Verbal Behavior Narration Language Tests Behavioral Symptoms Language Development Stanford-Binet Test

Phenomena and Processes22

Trinucleotide Repeats Trinucleotide Repeat Expansion Sex Chromosome Aberrations Mutation Mosaicism X Chromosome Repetitive Sequences, Nucleic Acid Chromosome Fragility Phenotype Heterozygote Alleles Base Sequence DNA Repeat Expansion Chromosome Fragile Sites Chromosomes, Human, Pair 19 Neuronal Plasticity Genetic Linkage Genetic Markers Protein Biosynthesis Alternative Splicing Chromosomes, Human, X Minisatellite Repeats

Disciplines and Occupations1

Genetic Counseling

Information Science5

Nonverbal Communication Base Sequence Molecular Sequence Data Narration Vocabulary

Health Care3

Genetic Testing Genetic Counseling Narration

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

Fragile X Syndrome Myotonic Dystrophy Fragile X Mental Retardation Protein Trinucleotide Repeats Trinucleotide Repeat Expansion Muscular Dystrophies RNA-Binding Proteins Syndrome Myotonic Disorders Sex Chromosome Aberrations Muscular Dystrophy, Duchenne Heterozygote Detection Intellectual Disability Pedigree Corneal Dystrophies, Hereditary Autistic Disorder Nerve Tissue Proteins Receptors, Metabotropic Glutamate Receptor, Metabotropic Glutamate 5 Genetic Testing Muscular Dystrophy, Animal Myotonia Mutation Mosaicism Down Syndrome Muscular Dystrophy, Facioscapulohumeral Disease Models, Animal Nonverbal Communication Methoxyhydroxyphenylglycol X Chromosome Repetitive Sequences, Nucleic Acid Chromosome Fragility Child Development Disorders, Pervasive Mice, Knockout Phenotype Fuchs' Endothelial Dystrophy Epilepsy, Reflex Ataxia Intelligence Tests Heterozygote Alleles Tremor Language Development Disorders Genetic Counseling Base Sequence Protein-Serine-Threonine Kinases Blotting, Southern DNA Repeat Expansion Dendritic Spines Molecular Sequence Data DNA Retinal Dystrophies Chromosome Fragile Sites Chromosomes, Human, Pair 19 Muscle, Skeletal Prenatal Diagnosis Lithium Compounds Intelligence Dystrophin Child Language Communication Disorders RNA, Messenger Polymerase Chain Reaction Brain DNA Mutational Analysis Verbal Behavior RNA Language Disorders Synapses Primary Ovarian Insufficiency Neuronal Plasticity Narration Genetic Linkage DNA Probes Vocabulary Language Tests Behavioral Symptoms Genetic Markers Protein Biosynthesis Alternative Splicing Language Development Stanford-Binet Test Dendrites Chromosomes, Human, X Neurons Myoblasts Metabolic Syndrome X Minisatellite Repeats Mice, Inbred C57BL Myotonia Congenita Muscular Dystrophy, Emery-Dreifuss

No FAQ available that match "fragile x syndrome and myotonic dystrophy"