Mutations in autism. Medical search. Frequent questions

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Anatomy15

Cell Line Brain COS Cells Cells, Cultured Chromosomes, Human, Pair 15 Chromosomes, Human, X Chromosomes, Human, Pair 16 Face X Chromosome HEK293 Cells Chromosomes, Human, Pair 7 Cell Line, Tumor HeLa Cells Fibroblasts Cerebral Cortex

Organisms11

Escherichia coli Saccharomyces cerevisiae Mice, Mutant Strains Mice, Inbred C57BL Mice, Transgenic Cercopithecus aethiops Drosophila melanogaster Cricetinae Mice, Knockout Drosophila HIV-1

Diseases21

Genetic Predisposition to Disease Language Development Disorders Intellectual Disability Syndrome Communication Disorders Fragile X Syndrome Rett Syndrome Abnormalities, Multiple Disease Models, Animal Chromosome Deletion Genetic Diseases, X-Linked Macrocephaly Retinitis Pigmentosa Eye Abnormalities Mitochondrial Diseases Language Disorders Craniofacial Abnormalities Genetic Diseases, Inborn Osteochondrodysplasias Facies Chromosome Duplication

Chemicals and Drugs53

Codon, Nonsense DNA Primers Codon DNA-Binding Proteins Transcription Factors Membrane Proteins DNA Mutant Proteins Bacterial Proteins DNA, Mitochondrial Carrier Proteins Nuclear Proteins Proto-Oncogene Proteins B-raf Nerve Tissue Proteins RNA, Messenger DNA, Neoplasm Genetic Markers Recombinant Proteins RNA Splice Sites Proteins Eye Proteins Methyl-CpG-Binding Protein 2 Mutagens Proto-Oncogene Proteins Saccharomyces cerevisiae Proteins Ethylnitrosourea Repressor Proteins Recombinant Fusion Proteins Tumor Suppressor Protein p53 BRCA2 Protein Fungal Proteins ras Proteins Escherichia coli Proteins DNA, Complementary Codon, Terminator Drosophila Proteins DNA, Bacterial DNA Transposable Elements Homeodomain Proteins Fragile X Mental Retardation Protein Trans-Activators Tumor Suppressor Proteins Membrane Transport Proteins Ethyl Methanesulfonate Adaptor Proteins, Signal Transducing Arginine Adenosine Triphosphatases Protein-Serine-Threonine Kinases Alanine Cell Adhesion Molecules, Neuronal Neoplasm Proteins Glycine Cysteine

Analytical, Diagnostic and Therapeutic Techniques and Equipment30

Pedigree Amino Acid Substitution DNA Mutational Analysis Polymerase Chain Reaction Mutagenesis, Site-Directed Sequence Analysis, DNA Genetic Testing Chromosome Mapping Models, Molecular Genetic Complementation Test Case-Control Studies Models, Genetic Cloning, Molecular Sequence Alignment Heterozygote Detection Transfection Mutagenesis, Insertional Genetic Association Studies Magnetic Resonance Imaging Disease Models, Animal Crosses, Genetic Restriction Mapping Reverse Transcriptase Polymerase Chain Reaction Cohort Studies Models, Biological Blotting, Western Immunohistochemistry Language Therapy Facies Facial Expression

Psychiatry and Psychology31

Autistic Disorder Asperger Syndrome Regression (Psychology)Social Behavior Intellectual Disability Stereotyped Behavior Developmental Disabilities Stereotypic Movement Disorder Communication Disorders Nonverbal Communication Siblings Verbal Behavior Intelligence Family Social Perception Imitative Behavior Neuropsychological Tests Parents Intelligence Tests Interpersonal Relations Attention Behavior Therapy Language Grooming Generalization (Psychology)Child Development Language Development Theory of Mind Communication Facial Expression Language Tests

Phenomena and Processes102

Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Mutation Rate Exons Base Sequence Heterozygote Amino Acid Substitution Alleles Genotype Polymorphism, Single-Stranded Conformational Amino Acid Sequence Homozygote Codon, Nonsense Phenotype Mutagenesis Genetic Predisposition to Disease Genes, Recessive Sequence Deletion Genes, Dominant Protein Structure, Tertiary Suppression, Genetic Genetic Linkage Gene Deletion Codon Sequence Homology, Amino Acid Binding Sites Founder Effect Genes, p53 Exome Protein Binding Genetic Variation Polymorphism, Genetic Consanguinity Plasmids Gene Frequency Transfection Polymorphism, Single Nucleotide Genes, Lethal Transcription, Genetic Introns Genes, BRCA1 Promoter Regions, Genetic Mutagenesis, Insertional Microsatellite Repeats Signal Transduction Genes, Bacterial Protein Conformation Genes Recombination, Genetic Genetic Markers Structure-Activity Relationship Drug Resistance, Viral Penetrance RNA Splice Sites Genes, Suppressor Genetic Heterogeneity Kinetics Conserved Sequence DNA Copy Number Variations Polymorphism, Restriction Fragment Length Chromosome Deletion INDEL Mutation Gene Dosage Temperature Evolution, Molecular Gene Expression Regulation Genes, BRCA2 RNA Splicing Selection, Genetic Genes, Fungal Gene Expression Protein Structure, Secondary DNA Repair Paternal Age Mosaicism Chromosomes, Human, Pair 15 Time Factors Codon, Terminator Chromosomes, Human, X DNA Transposable Elements Drug Resistance, Microbial Phosphorylation Amino Acid Motifs Chromosomes, Human, Pair 16 Loss of Heterozygosity X Chromosome Protein Transport Gene Expression Regulation, Bacterial Endophenotypes Chromosomes, Human, Pair 7 Virus Replication Child Development Drug Resistance Alternative Splicing Chromosome Duplication Gene Duplication Phylogeny Genes, APC Gene Expression Regulation, Developmental

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena7

Play and Playthings Siblings Family Education, Special Parents Social Behavior Disorders Mainstreaming (Education)

Information Science7

Base Sequence Molecular Sequence Data Amino Acid Sequence Nonverbal Communication Language Communication Phylogeny

Named Groups5

Siblings Jews Asian Continental Ancestry Group Parents Infant, Newborn

Health Care7

Genetic Testing Family Health Case-Control Studies Age of Onset Temperature Cohort Studies Early Intervention (Education)

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 Named Groups Health Care

Autistic Disorder Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Pedigree Asperger Syndrome Mutation Rate Exons Base Sequence Heterozygote Amino Acid Substitution DNA Mutational Analysis Alleles Polymerase Chain Reaction Molecular Sequence Data Genotype Polymorphism, Single-Stranded Conformational Mutagenesis, Site-Directed Amino Acid Sequence Regression (Psychology)Homozygote Codon, Nonsense Phenotype Sequence Analysis, DNA Mutagenesis Social Behavior Genetic Predisposition to Disease Genes, Recessive Genetic Testing Language Development Disorders Sequence Deletion Intellectual Disability Chromosome Mapping Genes, Dominant Protein Structure, Tertiary DNA Primers Escherichia coli Suppression, Genetic Models, Molecular Genetic Linkage Stereotyped Behavior Gene Deletion Cell Line Codon Syndrome DNA-Binding Proteins Developmental Disabilities Sequence Homology, Amino Acid Binding Sites Transcription Factors Genetic Complementation Test Stereotypic Movement Disorder Communication Disorders Family Health Membrane Proteins Case-Control Studies Models, Genetic Founder Effect Genes, p53 Cloning, Molecular Exome DNA Protein Binding Sequence Alignment Brain Nonverbal Communication Play and Playthings Mutant Proteins Genetic Variation Siblings Saccharomyces cerevisiae Polymorphism, Genetic Consanguinity Bacterial Proteins Plasmids Fragile X Syndrome Gene Frequency Heterozygote Detection Transfection Polymorphism, Single Nucleotide DNA, Mitochondrial Carrier Proteins Nuclear Proteins Genes, Lethal Transcription, Genetic Introns Age of Onset Proto-Oncogene Proteins B-raf Genes, BRCA1 Promoter Regions, Genetic Mutagenesis, Insertional Genetic Association Studies Microsatellite Repeats Nerve Tissue Proteins RNA, Messenger Rett Syndrome DNA, Neoplasm Signal Transduction

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