Sources abnormalities multiple. Medical search. Frequent questions

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Anatomy41

Brain Cells, Cultured Cerebral Cortex Chromosomes, Human, Pair 13 Heart Liver Kidney Chromosomes, Human, Pair 11 Nerve Fibers, Myelinated Lung Skin Fetus Neurons Chromosomes, Human, Pair 7 Bone Marrow Myocardium Bone and Bones Corpus Callosum Heart Ventricles Temporal Lobe Spermatozoa Embryo, Mammalian Cerebellum Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 18 Frontal Lobe Chromosomes, Human, Pair 14 Cell Line Feces Chromosomes, Human, Pair 8 Retina Chromosomes, Human, Pair 5 Chromosomes, Human, 6-12 and X Skull Chromosomes, Human, Pair 1 Muscle, Skeletal Neural Pathways Fibroblasts Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 12 Mitochondria

Organisms10

Mice, Knockout Mice, Inbred C57BL Mice, Transgenic Mice, Mutant Strains Cattle Animals, Newborn Dogs Swine Rats, Sprague-Dawley Escherichia coli

Diseases58

Abnormalities, Multiple Chromosome Aberrations Congenital Abnormalities Chromosome Disorders Eye Abnormalities Cardiovascular Abnormalities Craniofacial Abnormalities Syndrome Skin Abnormalities Urogenital Abnormalities Trisomy Musculoskeletal Abnormalities Tooth Abnormalities Disease Models, Animal Aneuploidy Translocation, Genetic Sex Chromosome Aberrations Abnormalities, Drug-Induced Fetal Diseases Brain Diseases Chromosome Deletion Heart Defects, Congenital Nervous System Malformations Intellectual Disability Down Syndrome Agenesis of Corpus Callosum Heart Diseases Atrophy Digestive System Abnormalities Acute Disease Limb Deformities, Congenital Myelodysplastic Syndromes Infertility, Male Ocular Motility Disorders Blood Coagulation Disorders Abnormal Karyotype Nervous System Diseases Disease Progression Chronic Disease Body Weight Arrhythmias, Cardiac Epilepsy Cardiomyopathies Monosomy Retinal Diseases Sturge-Weber Syndrome Maxillofacial Abnormalities Respiratory System Abnormalities Fetal Death Jaw Abnormalities Hypertension Metabolic Diseases Seizures Eye Diseases Leukemia, Myeloid, Acute Recurrence Neoplasms Turner Syndrome

Chemicals and Drugs20

Carbon Nitrogen RNA, Messenger Culture Media Glucose Biological Markers Transcription Factors DNA Primers DNA-Binding Proteins DNA, Bacterial Membrane Proteins DNA Nerve Tissue Proteins Amino Acids Blood Glucose Oxygen Fatty Acids Lipids Dietary Proteins Bacterial Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment70

Karyotyping Magnetic Resonance Imaging In Situ Hybridization, Fluorescence Retrospective Studies Sensitivity and Specificity Disease Models, Animal Case-Control Studies Electrocardiography Prospective Studies Risk Factors Reproducibility of Results Tomography, X-Ray Computed Electroencephalography Pedigree Follow-Up Studies Cytogenetic Analysis Analysis of Variance Polymerase Chain Reaction Reference Values Ultrasonography, Prenatal Prognosis Prenatal Diagnosis Chromosome Banding Echocardiography Predictive Value of Tests Immunohistochemistry Prevalence Sequence Analysis, DNA Brain Mapping Biopsy Culture Media Treatment Outcome Models, Biological Cohort Studies Severity of Illness Index Diffusion Magnetic Resonance Imaging Neurologic Examination Chromosome Mapping Microscopy, Electron Tomography, Emission-Computed, Single-Photon Cross-Sectional Studies Body Weight DNA Mutational Analysis Reverse Transcriptase Polymerase Chain Reaction Gene Expression Profiling Incidence Magnetoencephalography Imaging, Three-Dimensional Gene Targeting Risk Assessment Organ Size Diffusion Tensor Imaging Observer Variation Electroretinography Radiography, Thoracic Statistics, Nonparametric Statistics as Topic Oligonucleotide Array Sequence Analysis Random Allocation In Situ Hybridization Regression Analysis Amniocentesis Magnetic Resonance Spectroscopy Ultrasonography Image Interpretation, Computer-Assisted Flow Cytometry Autopsy Cluster Analysis Chi-Square Distribution Blood Pressure

Psychiatry and Psychology9

Schizophrenia Intellectual Disability Neuropsychological Tests Functional Laterality Developmental Disabilities Behavior, Animal Dominance, Cerebral Autistic Disorder Cognition Disorders

Phenomena and Processes59

Chromosome Aberrations Phenotype Mutation Pregnancy Time Factors Trisomy Sensitivity and Specificity Aneuploidy Translocation, Genetic Base Sequence Sex Chromosome Aberrations Chromosome Deletion Heterozygote Homozygote Gene Deletion Genotype Amino Acid Sequence Chromosomes, Human, Pair 13 Gestational Age Phylogeny Mosaicism Cell Differentiation Chromosomes, Human, Pair 11 Gene Expression Abnormal Karyotype Signal Transduction Diet Anisotropy Aging Chromosomes, Human, Pair 7 Gene Expression Regulation, Developmental Body Weight Species Specificity Functional Laterality Organ Size Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 18 Monosomy Kinetics Gene Expression Regulation Alleles Dominance, Cerebral Chromosomes, Human, Pair 14 Energy Metabolism Genetic Variation Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 5 Chromosomes, Human, 6-12 and X Chromosomes, Human, Pair 1 Neural Conduction Hydrogen-Ion Concentration Oxidation-Reduction Chi-Square Distribution Embryonic and Fetal Development Chromosomes, Human, Pair 3 Genes, Recessive Blood Pressure Chromosomes, Human, Pair 12 Dose-Response Relationship, Drug

Disciplines and Occupations5

Cytogenetics Immunohistochemistry Water Microbiology Water Supply Statistics as Topic

Anthropology, Education, Sociology and Social Phenomena1

Technology, Industry, Agriculture2

Animal Feed Dietary Proteins

Information Science11

Molecular Sequence Data Image Processing, Computer-Assisted Base Sequence Prevalence Amino Acid Sequence Phylogeny Incidence Imaging, Three-Dimensional Databases, Factual Image Interpretation, Computer-Assisted Computer Simulation

Named Groups1

Infant, Newborn

Health Care29

Retrospective Studies Sensitivity and Specificity Case-Control Studies Prospective Studies Risk Factors Reproducibility of Results Follow-Up Studies Analysis of Variance Predictive Value of Tests Prevalence Age Factors Treatment Outcome Cohort Studies Severity of Illness Index Water Microbiology Cross-Sectional Studies Environmental Monitoring Incidence Risk Assessment Water Pollution Observer Variation Statistics, Nonparametric Statistics as Topic Random Allocation Environmental Exposure Sex Factors Regression Analysis Cluster Analysis Chi-Square Distribution

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Abnormalities, Multiple Chromosome Aberrations Congenital Abnormalities Chromosome Disorders Karyotyping Eye Abnormalities Magnetic Resonance Imaging Brain Phenotype Mutation Pregnancy Cardiovascular Abnormalities Time Factors Craniofacial Abnormalities Syndrome Skin Abnormalities Molecular Sequence Data Urogenital Abnormalities Infant, Newborn Trisomy In Situ Hybridization, Fluorescence Musculoskeletal Abnormalities Tooth Abnormalities Retrospective Studies Sensitivity and Specificity Disease Models, Animal Case-Control Studies Aneuploidy Electrocardiography Image Processing, Computer-Assisted Translocation, Genetic Base Sequence Prospective Studies Risk Factors Reproducibility of Results Mice, Knockout Tomography, X-Ray Computed Mice, Inbred C57BL Electroencephalography Sex Chromosome Aberrations Schizophrenia Abnormalities, Drug-Induced Fetal Diseases Pedigree Carbon Mice, Transgenic Follow-Up Studies Brain Diseases Cytogenetic Analysis Analysis of Variance Nitrogen Polymerase Chain Reaction Chromosome Deletion Reference Values Heart Defects, Congenital Ultrasonography, Prenatal Cells, Cultured Mice, Mutant Strains Prognosis Prenatal Diagnosis Chromosome Banding Cytogenetics Echocardiography Heterozygote Predictive Value of Tests Nervous System Malformations Homozygote Immunohistochemistry Prevalence RNA, Messenger Sequence Analysis, DNA Age Factors Gene Deletion Brain Mapping Biopsy Intellectual Disability Genotype Culture Media Treatment Outcome Cerebral Cortex Amino Acid Sequence Models, Biological Chromosomes, Human, Pair 13 Cohort Studies Heart Glucose Down Syndrome Liver United States Gestational Age Agenesis of Corpus Callosum Heart Diseases Biological Markers Atrophy Phylogeny Digestive System Abnormalities Severity of Illness Index Acute Disease Mosaicism Diffusion Magnetic Resonance Imaging

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