Developmental abnormalities multiple. Medical search. Frequent questions

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Anatomy42

Embryo, Mammalian Brain Embryo, Nonmammalian Blastocyst Cells, Cultured Neurons Kidney Cell Line 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 Heart Ventricles Chromosomes, Human, Pair 14 Bone Marrow Cerebellum Spermatozoa Fetus 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 Skin Frontal Lobe Liver Chromosomes, Human, X Chromosomes, Human, Pair 21 Skull Chromosomes, Human, 13-15 Cerebral Ventricles Retina

Organisms11

Zebrafish Mice, Mutant Strains Mice, Knockout Plants, Genetically Modified Mice, Transgenic Arabidopsis Mice, Inbred C57BL Animals, Genetically Modified Animals, Newborn Mice, Neurologic Mutants Dogs

Diseases73

Congenital Abnormalities Abnormalities, Multiple Eye Abnormalities Choristoma Skin Abnormalities Limb Deformities, Congenital Craniofacial Abnormalities Syndrome Smith-Lemli-Opitz Syndrome Fanconi Anemia Cockayne Syndrome Disease Models, Animal Heart Defects, Congenital Chromosome Aberrations Chromosome Disorders Cardiovascular Abnormalities Urogenital Abnormalities Trisomy Musculoskeletal Abnormalities Tooth Abnormalities Translocation, Genetic Aneuploidy Sex Chromosome Aberrations Abnormalities, Drug-Induced Fetal Diseases Brain Diseases Chromosome Deletion Nervous System Malformations Intellectual Disability Agenesis of Corpus Callosum Down Syndrome Digestive System Abnormalities Atrophy 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 Blood Platelet Disorders Lymphatic Abnormalities Sex Chromosome Disorders of Sex Development

Chemicals and Drugs15

Zebrafish Proteins Transcription Factors DNA-Binding Proteins Arabidopsis Proteins Homeodomain Proteins Paired Box Transcription Factors RNA, Messenger DNA Primers Drosophila Proteins Trans-Activators Membrane Proteins Proteins DNA Biological Markers Nerve Tissue Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment58

Gene Targeting Cloning, Organism Disease Models, Animal Pedigree Magnetic Resonance Imaging In Situ Hybridization Chromosome Mapping Gene Knockdown Techniques Immunohistochemistry Models, Biological Karyotyping In Situ Hybridization, Fluorescence Electrocardiography Retrospective Studies Case-Control Studies 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 Severity of Illness Index Prevalence Cohort Studies Treatment Outcome Tomography, Emission-Computed, Single-Photon Reproducibility of Results DNA Mutational Analysis Polymerase Chain Reaction Diffusion Tensor Imaging Brain Mapping Electroretinography Microscopy, Electron Radiography, Thoracic Amniocentesis Organ Size Echoencephalography Observer Variation Ultrasonography Imaging, Three-Dimensional Vaginal Smears Body Weight Blood Pressure Statistics, Nonparametric Autopsy Chi-Square Distribution

Psychiatry and Psychology9

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

Phenomena and Processes71

Phenotype Mutation Gene Expression Regulation, Developmental Embryonic and Fetal Development Plant Infertility Pregnancy Base Sequence Homozygote Embryonic Development Transgenes Morphogenesis Amino Acid Sequence Body Patterning Gene Deletion Gene Silencing Cell Differentiation Gene Expression Regulation, Plant Gene Expression Alleles Signal Transduction Exons DNA Repair Chromosome Aberrations Apoptosis Gene Expression Regulation Sequence Homology, Amino Acid Time Factors Cell Division Promoter Regions, Genetic Transcription, Genetic Trisomy Translocation, Genetic Aneuploidy Sex Chromosome Aberrations Chromosome Deletion Sensitivity and Specificity Heterozygote Chromosomes, Human, Pair 13 Mosaicism Chromosomes, Human, Pair 11 Gestational Age Abnormal Karyotype Chromosomes, Human, Pair 7 Anisotropy Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 18 Monosomy Chromosomes, Human, Pair 14 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 Body Weight Blood Pressure Ploidies Chromosomes, Human, 13-15 Chi-Square Distribution

Disciplines and Occupations2

Immunohistochemistry Cytogenetics

Anthropology, Education, Sociology and Social Phenomena1

Information Science6

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

Named Groups1

Infant, Newborn

Health Care17

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 Statistics, Nonparametric Chi-Square Distribution

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

Congenital Abnormalities Abnormalities, Multiple Eye Abnormalities Phenotype Mutation Gene Expression Regulation, Developmental Choristoma Skin Abnormalities Embryonic and Fetal Development Developmental Disabilities Gene Targeting Embryo, Mammalian Limb Deformities, Congenital Zebrafish Craniofacial Abnormalities Plant Infertility Mice, Mutant Strains Pregnancy Cloning, Organism Syndrome Smith-Lemli-Opitz Syndrome Molecular Sequence Data Fanconi Anemia Base Sequence Homozygote Embryonic Development Zebrafish Proteins Mice, Knockout Brain Embryo, Nonmammalian Cockayne Syndrome Plants, Genetically Modified Transcription Factors Mice, Transgenic Arabidopsis Mice, Inbred C57BL Autistic Disorder Transgenes DNA-Binding Proteins Morphogenesis Disease Models, Animal Amino Acid Sequence Arabidopsis Proteins Homeodomain Proteins Body Patterning Heart Defects, Congenital Gene Deletion Paired Box Transcription Factors Pedigree Infant, Newborn Magnetic Resonance Imaging RNA, Messenger In Situ Hybridization Gene Silencing Chromosome Mapping Gene Knockdown Techniques Animals, Genetically Modified Cell Differentiation Blastocyst DNA Primers Gene Expression Regulation, Plant Gene Expression Alleles Signal Transduction Exons Animals, Newborn Drosophila Proteins Trans-Activators DNA Repair Chromosome Aberrations Immunohistochemistry Apoptosis Gene Expression Regulation Cells, Cultured Neurons Sequence Homology, Amino Acid Time Factors Membrane Proteins Kidney Proteins Cell Line Models, Biological Cell Division DNA Chromosome Disorders Promoter Regions, Genetic Karyotyping Transcription, Genetic Cardiovascular Abnormalities Urogenital Abnormalities Trisomy Musculoskeletal Abnormalities In Situ Hybridization, Fluorescence Tooth Abnormalities Translocation, Genetic Aneuploidy Electrocardiography Sex Chromosome Aberrations Retrospective Studies Abnormalities, Drug-Induced

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