Gene abnormalities. Medical search. Frequent questions

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Anatomy36

Brain Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 11 Nerve Fibers, Myelinated Heart Chromosomes, Human, Pair 7 Cerebral Cortex Corpus Callosum Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 18 Kidney Heart Ventricles Chromosomes, Human, Pair 14 Bone Marrow Cerebellum Spermatozoa Fetus Cells, Cultured Chromosomes, Human, 6-12 and X Temporal Lobe Chromosomes, Human, Pair 8 Lung Myocardium Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 1 Bone and Bones Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 12 Embryo, Mammalian Skin Frontal Lobe Liver Chromosomes, Human, X Chromosomes, Human, Pair 21 Skull Chromosomes, Human, 13-15

Organisms6

Mice, Knockout Mice, Transgenic Mice, Mutant Strains Mice, Inbred C57BL Animals, Newborn Mice, Neurologic Mutants

Diseases66

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

Chemicals and Drugs5

Cyclin-Dependent Kinase Inhibitor p16 Biological Markers RNA, Messenger Transcription Factors Nerve Tissue Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment51

DNA Mutational Analysis Polymerase Chain Reaction Karyotyping Magnetic Resonance Imaging In Situ Hybridization, Fluorescence Electrocardiography Disease Models, Animal Retrospective Studies Case-Control Studies Pedigree Prospective Studies Cytogenetic Analysis Tomography, X-Ray Computed Ultrasonography, Prenatal Sensitivity and Specificity Chromosome Banding Follow-Up Studies Prenatal Diagnosis Echocardiography Prognosis Risk Factors Reference Values Biopsy Predictive Value of Tests Electroencephalography Neurologic Examination Diffusion Magnetic Resonance Imaging Analysis of Variance Immunohistochemistry Severity of Illness Index Prevalence Cohort Studies Treatment Outcome Tomography, Emission-Computed, Single-Photon Reproducibility of Results Diffusion Tensor Imaging Gene Targeting Brain Mapping Electroretinography Microscopy, Electron Radiography, Thoracic Amniocentesis Organ Size Chromosome Mapping Echoencephalography Observer Variation Ultrasonography Imaging, Three-Dimensional Vaginal Smears Body Weight Blood Pressure

Psychiatry and Psychology9

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

Phenomena and Processes53

Polymorphism, Single-Stranded Conformational Mutation Gene Deletion Chromosome Aberrations Phenotype Pregnancy Trisomy Translocation, Genetic Aneuploidy Sex Chromosome Aberrations Time Factors Chromosome Deletion Sensitivity and Specificity Homozygote Heterozygote Chromosomes, Human, Pair 13 Mosaicism Chromosomes, Human, Pair 11 Gestational Age Abnormal Karyotype Chromosomes, Human, Pair 7 Base Sequence Anisotropy Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 18 Monosomy Chromosomes, Human, Pair 14 Gene Expression Regulation, Developmental Chromosomes, Human, 6-12 and X Dominance, Cerebral Chromosomes, Human, Pair 8 Genotype Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 1 Aging Chromosomes, Human, Pair 3 Organ Size Chromosomes, Human, Pair 12 Neural Conduction Genes, Recessive Gene Rearrangement Chromosomes, Human, X Myocardial Contraction Functional Laterality Chromosomes, Human, Pair 21 Pregnancy Trimester, Second Gene Expression Body Weight Embryonic and Fetal Development Blood Pressure Ploidies Chromosomes, Human, 13-15 Signal Transduction

Disciplines and Occupations2

Cytogenetics Immunohistochemistry

Information Science5

Image Processing, Computer-Assisted Molecular Sequence Data Base Sequence Prevalence Imaging, Three-Dimensional

Named Groups1

Infant, Newborn

Health Care15

Retrospective Studies Case-Control Studies Prospective Studies Sensitivity and Specificity Follow-Up Studies Risk Factors Predictive Value of Tests Analysis of Variance Severity of Illness Index Prevalence Cohort Studies Age Factors Treatment Outcome Reproducibility of Results Observer Variation

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

Polymorphism, Single-Stranded Conformational Cyclin-Dependent Kinase Inhibitor p16 Mutation Gene Deletion DNA Mutational Analysis Polymerase Chain Reaction Abnormalities, Multiple Chromosome Aberrations Congenital Abnormalities Chromosome Disorders Eye Abnormalities Karyotyping Magnetic Resonance Imaging Brain Cardiovascular Abnormalities Craniofacial Abnormalities Syndrome Skin Abnormalities Phenotype Urogenital Abnormalities Pregnancy Trisomy Musculoskeletal Abnormalities In Situ Hybridization, Fluorescence Tooth Abnormalities Translocation, Genetic Infant, Newborn Aneuploidy Electrocardiography Disease Models, Animal Sex Chromosome Aberrations Retrospective Studies Abnormalities, Drug-Induced Case-Control Studies Time Factors Fetal Diseases Schizophrenia Pedigree Prospective Studies Cytogenetic Analysis Brain Diseases Tomography, X-Ray Computed Mice, Knockout Ultrasonography, Prenatal Chromosome Deletion Heart Defects, Congenital Sensitivity and Specificity Image Processing, Computer-Assisted Chromosome Banding Follow-Up Studies Cytogenetics Prenatal Diagnosis Nervous System Malformations Echocardiography Mice, Transgenic Mice, Mutant Strains Prognosis Homozygote Risk Factors Mice, Inbred C57BL Heterozygote Intellectual Disability Chromosomes, Human, Pair 13 Reference Values Biopsy Predictive Value of Tests Agenesis of Corpus Callosum Down Syndrome Digestive System Abnormalities Electroencephalography Atrophy Limb Deformities, Congenital Mosaicism Chromosomes, Human, Pair 11 Neurologic Examination Diffusion Magnetic Resonance Imaging Ocular Motility Disorders Myelodysplastic Syndromes Gestational Age Abnormal Karyotype Nerve Fibers, Myelinated Heart Infertility, Male Analysis of Variance Blood Coagulation Disorders Chromosomes, Human, Pair 7 Cerebral Cortex Immunohistochemistry Severity of Illness Index Heart Diseases Molecular Sequence Data Base Sequence Prevalence Nervous System Diseases Corpus Callosum Cohort Studies Acute Disease Age Factors Treatment Outcome Tomography, Emission-Computed, Single-Photon

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