Neurodevelopmental disorder angelman syndrome. Medical search. Frequent questions

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Anatomy4

Chromosomes, Human, Pair 15 Brain Neurons Neural Pathways

Organisms2

Mice, Knockout Mice, Inbred C57BL

Diseases29

Angelman Syndrome Prader-Willi Syndrome Rett Syndrome Syndrome Intellectual Disability Williams Syndrome Uniparental Disomy Microcephaly Nervous System Diseases Chromosome Deletion Beckwith-Wiedemann Syndrome Disease Models, Animal Abnormalities, Multiple Chromosome Inversion Ataxia Epilepsy Prenatal Exposure Delayed Effects Chromosome Breakage Language Development Disorders Learning Disorders Neuronal Migration Disorders Tourette Syndrome Psychomotor Disorders Fetal Alcohol Spectrum Disorders Communication Disorders Down Syndrome Genetic Predisposition to Disease Brain Diseases Fragile X Syndrome

Chemicals and Drugs7

Methyl-CpG-Binding Protein 2 snRNP Core Proteins Ubiquitin-Protein Ligases Ribonucleoproteins, Small Nuclear Nerve Tissue Proteins Genetic Markers Autoantigens

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

Disease Models, Animal Pedigree Chromosome Mapping In Situ Hybridization, Fluorescence Magnetic Resonance Imaging Chromosome Banding

Psychiatry and Psychology17

Developmental Disabilities Autistic Disorder Child Development Disorders, Pervasive Intellectual Disability Laughter Child Development Mental Disorders Schizophrenia Attention Deficit Disorder with Hyperactivity Bipolar Disorder Learning Disorders Tourette Syndrome Fathers Psychomotor Disorders Communication Disorders Cognition Disorders Stereotyped Behavior

Phenomena and Processes18

Chromosomes, Human, Pair 15 Genomic Imprinting Uniparental Disomy Chromosome Deletion Phenotype Child Development DNA Methylation Mutation Chromosome Inversion Genetic Markers Chromosome Breakage Pregnancy Gene Dosage Genotype Sequence Deletion Gene Deletion DNA Copy Number Variations Genetic Predisposition to Disease

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Fathers Social Behavior Disorders

Named Groups3

Infant, Newborn Fathers Infant, Extremely Low Birth Weight

Health Care1

Genetic Counseling

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 Named Groups Health Care

Angelman Syndrome Prader-Willi Syndrome Chromosomes, Human, Pair 15 Rett Syndrome Developmental Disabilities Methyl-CpG-Binding Protein 2 Genomic Imprinting snRNP Core Proteins Autistic Disorder Syndrome Ubiquitin-Protein Ligases Child Development Disorders, Pervasive Intellectual Disability Williams Syndrome Uniparental Disomy Brain Microcephaly Nervous System Diseases Laughter Chromosome Deletion Phenotype Ribonucleoproteins, Small Nuclear Beckwith-Wiedemann Syndrome Disease Models, Animal Abnormalities, Multiple Child Development DNA Methylation Pedigree Mental Disorders Mutation Chromosome Inversion Schizophrenia Infant, Newborn Chromosome Mapping In Situ Hybridization, Fluorescence Ataxia Neurons Attention Deficit Disorder with Hyperactivity Epilepsy Nerve Tissue Proteins Prenatal Exposure Delayed Effects Genetic Markers Chromosome Breakage Pregnancy Magnetic Resonance Imaging Language Development Disorders Bipolar Disorder Genetic Counseling Learning Disorders Chromosome Banding Mice, Knockout Gene Dosage Genotype Neuronal Migration Disorders Tourette Syndrome Sequence Deletion Autoantigens Fathers Psychomotor Disorders Mice, Inbred C57BL Fetal Alcohol Spectrum Disorders Communication Disorders Gene Deletion Cognition Disorders DNA Copy Number Variations Social Behavior Disorders Down Syndrome Genetic Predisposition to Disease Brain Diseases Infant, Extremely Low Birth Weight Fragile X Syndrome Neural Pathways Stereotyped Behavior

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