Morphological abnormalities induced. Medical search. Frequent questions

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Anatomy47

Spermatozoa Brain Embryo, Mammalian Embryo, Nonmammalian Testis Mitochondria Bone Marrow Neurons Cells, Cultured 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 Cerebellum 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 Chromosomes, Human, Pair 6 Neck X Chromosome Chromosomes, Human, Pair 22 Erythrocytes, Abnormal

Organisms9

Mice, Mutant Strains Mice, Knockout Mice, Transgenic Zebrafish Mice, Inbred C57BL Animals, Newborn Rats, Sprague-Dawley Mice, Neurologic Mutants Dogs

Diseases78

Syndrome Infertility, Male Disease Models, Animal Abnormalities, Multiple Chromosome Aberrations Congenital Abnormalities Chromosome Disorders Eye Abnormalities Cardiovascular Abnormalities Craniofacial Abnormalities Skin Abnormalities Urogenital Abnormalities Trisomy Musculoskeletal Abnormalities Tooth Abnormalities Translocation, Genetic Aneuploidy 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 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 Klinefelter Syndrome Recurrence Reflex, Abnormal Uterine Cervical Neoplasms Leukemia, Myeloid Leukoencephalopathies Peripheral Nervous System Diseases Epilepsy, Temporal Lobe Azoospermia

Chemicals and Drugs8

Membrane Proteins DNA Primers Transcription Factors RNA, Messenger Biological Markers Nerve Tissue Proteins DNA-Binding Proteins Blood Glucose

Analytical, Diagnostic and Therapeutic Techniques and Equipment66

Microscopy, Electron Sperm Motility Radionuclide Ventriculography Magnetic Resonance Imaging Sperm Count Microscopy, Electron, Scanning Disease Models, Animal Immunohistochemistry In Situ Hybridization Karyotyping In Situ Hybridization, Fluorescence Electrocardiography 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 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 Gene Targeting Brain Mapping Electroretinography Radiography, Thoracic Amniocentesis Organ Size Chromosome Mapping Echoencephalography Observer Variation Ultrasonography Imaging, Three-Dimensional Vaginal Smears Body Weight Blood Pressure Statistics, Nonparametric Autopsy Chi-Square Distribution Magnetic Resonance Angiography Cross-Sectional Studies Reverse Transcriptase Polymerase Chain Reaction Reflex, Abnormal Comparative Genomic Hybridization Incidence Neuroimaging

Psychiatry and Psychology10

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

Phenomena and Processes68

Mutation Phenotype Sperm Motility Genes, Lethal Morphogenesis Sperm Count Gene Expression Regulation, Developmental Spermatogenesis Homozygote Time Factors Pregnancy Base Sequence Gene Deletion Amino Acid Sequence Cell Differentiation Gene Expression Apoptosis Chromosome Aberrations 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 Embryonic and Fetal Development Blood Pressure Ploidies Chromosomes, Human, 13-15 Signal Transduction Alleles Chi-Square Distribution Chromosomes, Human, Pair 6 Reflex, Abnormal Gene Dosage X Chromosome Mutation, Missense Chromosomes, Human, Pair 22

Disciplines and Occupations2

Immunohistochemistry Cytogenetics

Anthropology, Education, Sociology and Social Phenomena1

Information Science7

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

Named Groups1

Infant, Newborn

Health Care19

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 Cross-Sectional Studies Incidence

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

Mutation Spermatozoa Phenotype Microscopy, Electron Sperm Motility Radionuclide Ventriculography Syndrome Mice, Mutant Strains Mice, Knockout Magnetic Resonance Imaging Genes, Lethal Morphogenesis Sperm Count Brain Infertility, Male Gene Expression Regulation, Developmental Microscopy, Electron, Scanning Spermatogenesis Embryo, Mammalian Disease Models, Animal Homozygote Mice, Transgenic Embryo, Nonmammalian Immunohistochemistry Zebrafish Time Factors Molecular Sequence Data Mice, Inbred C57BL Pregnancy In Situ Hybridization Testis Animals, Newborn Mitochondria Base Sequence Gene Deletion Bone Marrow Membrane Proteins DNA Primers Neurons Amino Acid Sequence Rats, Sprague-Dawley Transcription Factors Cell Differentiation Gene Expression Abnormalities, Multiple RNA, Messenger Apoptosis Cells, Cultured Chromosome Aberrations Congenital Abnormalities Chromosome Disorders Eye Abnormalities Karyotyping Cardiovascular Abnormalities Craniofacial Abnormalities Skin Abnormalities Urogenital Abnormalities Trisomy Musculoskeletal Abnormalities In Situ Hybridization, Fluorescence Tooth Abnormalities Translocation, Genetic Infant, Newborn Aneuploidy Electrocardiography Sex Chromosome Aberrations Retrospective Studies Abnormalities, Drug-Induced Case-Control Studies Fetal Diseases Schizophrenia Pedigree Prospective Studies Cytogenetic Analysis Brain Diseases Tomography, X-Ray Computed 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 Prognosis Risk Factors 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

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