Diagnostic prenatal diagnosis. Medical search. Frequent questions

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Anatomy20

Amniotic Fluid Fetus Fetal Heart Chorionic Villi Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 13 Fetal Blood X Chromosome Chromosomes, Human, Pair 21 Umbilical Cord Cloaca Azygos Vein Chromosomes, Human, Pair 22 Sacrococcygeal Region Neck Chromosomes, Human, X Placenta Foramen Ovale Thorax Brain

Diseases105

Fetal Diseases Prenatal Exposure Delayed Effects Abnormalities, Multiple Chromosome Disorders Thalassemia Trisomy Down Syndrome Hydrops Fetalis Fetal Death Sex Chromosome Disorders Hemoglobinopathies Heart Defects, Congenital Congenital Abnormalities Polyhydramnios Syndrome Ectromelia Hernia, Umbilical beta-Thalassemia Genetic Diseases, Inborn Sex Chromosome Aberrations Twins, Conjoined Chromosome Aberrations Aneuploidy Prenatal Injuries Hydrocolpos Musculoskeletal Abnormalities Dandy-Walker Syndrome Levocardia Pulmonary Atresia Gastroschisis Adrenal Hyperplasia, Congenital Fetomaternal Transfusion Anus, Imperforate Muscular Dystrophies Hernia, Diaphragmatic Spinal Muscular Atrophies of Childhood Anencephaly Oligohydramnios Agenesis of Corpus Callosum Pregnancy Complications Neural Tube Defects Cystic Adenomatoid Malformation of Lung, Congenital Spinal Dysraphism Hydronephrosis Hypoplastic Left Heart Syndrome Micrognathism Toxoplasmosis, Congenital Amniotic Band Syndrome Encephalocele Meningomyelocele Bone Diseases, Developmental Intestinal Atresia Metabolism, Inborn Errors Heart Septal Defects Rare Diseases Citrullinemia alpha-Thalassemia Lymphangioma, Cystic Meningocele Amino Acid Metabolism, Inborn Errors Respiratory System Abnormalities Cystic Fibrosis Urogenital Abnormalities Hemophilia A Holoprosencephaly Ornithine Carbamoyltransferase Deficiency Disease Hypophosphatasia Spina Bifida Occulta Lymphangioma XYY Karyotype Hydrocephalus Thoracic Diseases Cri-du-Chat Syndrome Epidermolysis Bullosa Tricuspid Atresia Clubfoot Fetal Alcohol Spectrum Disorders Klippel-Trenaunay-Weber Syndrome Bronchopulmonary Sequestration Foot Deformities, Congenital Microcephaly Lipidoses Arthrogryposis Intellectual Disability Ichthyosis, Lamellar Anemia, Sickle Cell 46, XY Disorders of Sex Development Chondrodysplasia Punctata Aortopulmonary Septal Defect Chromosome Deletion Bladder Exstrophy Cysts Polydactyly Pregnancy Complications, Infectious Hemophilia B Prune Belly Syndrome Aortic Arch Syndromes Klinefelter Syndrome Arteriovenous Malformations Skin Abnormalities Cleft Lip Turner Syndrome Ectodermal Dysplasia Diseases in Twins Placenta Accreta

Chemicals and Drugs9

Genetic Markers DNA Reagent Kits, Diagnostic Steroid 21-Hydroxylase Biological Markers Globins DNA Probes alpha-Fetoproteins alpha-Globins

Analytical, Diagnostic and Therapeutic Techniques and Equipment77

Prenatal Diagnosis Ultrasonography, Prenatal Chorionic Villi Sampling Prenatal Care Amniocentesis Abortion, Eugenic Heterozygote Detection Abortion, Therapeutic Sensitivity and Specificity Abortion, Induced Pregnancy Outcome Genetic Testing Cordocentesis Karyotyping Diagnostic Errors Retrospective Studies Pedigree Polymerase Chain Reaction Preimplantation Diagnosis Ultrasonography, Doppler, Color Delayed Diagnosis Sex Determination Analysis Reproducibility of Results Early Diagnosis Fatal Outcome Fetoscopy Predictive Value of Tests Diagnostic Tests, Routine Prospective Studies Diagnosis Magnetic Resonance Imaging Diagnostic Techniques and Procedures Diagnostic Imaging Echocardiography, Four-Dimensional Biopsy DNA Mutational Analysis Molecular Diagnostic Techniques Risk Factors Ultrasonography Tomography, X-Ray Computed Imaging, Three-Dimensional Reagent Kits, Diagnostic Follow-Up Studies Prognosis Abortion, Legal False Positive Reactions Prevalence In Situ Hybridization, Fluorescence Cohort Studies Ultrasonography, Doppler, Pulsed ROC Curve Diagnosis, Computer-Assisted False Negative Reactions Neonatal Screening Clinical Enzyme Tests Treatment Outcome Autopsy Questionnaires Evaluation Studies as Topic Nuchal Translucency Measurement Incidence Echoencephalography Clinical Laboratory Techniques Cesarean Section Case-Control Studies Echocardiography Biopsy, Needle Mass Screening Postnatal Care Risk Assessment Ultrasonography, Doppler Registries Sequence Analysis, DNA Risk Logistic Models Enzyme-Linked Immunosorbent Assay Comparative Genomic Hybridization

Psychiatry and Psychology4

Mothers Maternal-Fetal Relations Intellectual Disability 46, XY Disorders of Sex Development

Phenomena and Processes40

Pregnancy Gestational Age Pregnancy Trimester, Second Sensitivity and Specificity Pregnancy Outcome Trisomy Pregnancy Trimester, First Pregnancy Trimester, Third Sex Chromosome Aberrations Chromosome Aberrations Aneuploidy Chromosomes, Human, Pair 18 Genetic Linkage Mosaicism Chromosomes, Human, Pair 13 Maternal Age Genetic Markers Pregnancy, High-Risk Polymorphism, Restriction Fragment Length Mutation Heterozygote Time Factors Maternal-Fetal Exchange X Chromosome Genes, Recessive Karyotype Chromosomes, Human, Pair 21 Consanguinity Chromosomes, Human, Pair 22 XYY Karyotype Base Sequence Pregnancy Trimesters Alleles Phenotype Genotype Chromosomes, Human, X Homozygote Polymorphism, Genetic Chromosome Deletion Risk

Disciplines and Occupations2

Genetic Counseling Perinatology

Anthropology, Education, Sociology and Social Phenomena2

Mothers Autopsy

Humanities2

Postmodernism Ethics, Medical

Information Science10

Fatal Outcome Imaging, Three-Dimensional Prevalence Diagnosis, Computer-Assisted Questionnaires Incidence Base Sequence Diagnostic and Statistical Manual of Mental Disorders Molecular Sequence Data Registries

Named Groups3

Infant, Newborn Pregnant Women Mothers

Health Care34

Prenatal Care Genetic Counseling Sensitivity and Specificity Genetic Testing Diagnostic Errors Retrospective Studies Reproducibility of Results Fatal Outcome Predictive Value of Tests Prospective Studies Genetic Services Maternal Age Risk Factors Maternal Exposure Follow-Up Studies Prevalence Cohort Studies ROC Curve Neonatal Screening Treatment Outcome Questionnaires Evaluation Studies as Topic Incidence Case-Control Studies Mass Screening Postnatal Care Nursing Diagnosis Risk Assessment Age Factors Registries Diagnostic Services Ethics, Medical Risk Logistic Models

Geographicals2

Israel United States

Anatomy 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 Humanities Information Science Named Groups Health Care Geographicals

Prenatal Diagnosis Fetal Diseases Ultrasonography, Prenatal Pregnancy Chorionic Villi Sampling Prenatal Exposure Delayed Effects Prenatal Care Amniocentesis Abortion, Eugenic Heterozygote Detection Genetic Counseling Infant, Newborn Abortion, Therapeutic Amniotic Fluid Gestational Age Pregnancy Trimester, Second Sensitivity and Specificity Abnormalities, Multiple Abortion, Induced Fetus Pregnancy Outcome Chromosome Disorders Genetic Testing Thalassemia Trisomy Cordocentesis Pregnancy Trimester, First Down Syndrome Hydrops Fetalis Karyotyping Diagnostic Errors Fetal Death Retrospective Studies Sex Chromosome Disorders Hemoglobinopathies Pedigree Heart Defects, Congenital Congenital Abnormalities Polyhydramnios Polymerase Chain Reaction Pregnancy Trimester, Third Preimplantation Diagnosis Ultrasonography, Doppler, Color Syndrome Ectromelia Hernia, Umbilical Delayed Diagnosis Pregnant Women Sex Determination Analysis beta-Thalassemia Fetal Heart Genetic Diseases, Inborn Reproducibility of Results Chorionic Villi Sex Chromosome Aberrations Early Diagnosis Twins, Conjoined Chromosome Aberrations Aneuploidy Fatal Outcome Chromosomes, Human, Pair 18 Fetoscopy Prenatal Injuries Predictive Value of Tests Diagnostic Tests, Routine Prospective Studies Hydrocolpos Diagnosis Magnetic Resonance Imaging Musculoskeletal Abnormalities Dandy-Walker Syndrome Genetic Linkage Mosaicism Diagnostic Techniques and Procedures Levocardia Pulmonary Atresia Gastroschisis Diagnostic Imaging Genetic Services Chromosomes, Human, Pair 13 Maternal Age Adrenal Hyperplasia, Congenital Fetomaternal Transfusion Genetic Markers Anus, Imperforate Echocardiography, Four-Dimensional DNA Biopsy Muscular Dystrophies DNA Mutational Analysis Molecular Diagnostic Techniques Hernia, Diaphragmatic Risk Factors Spinal Muscular Atrophies of Childhood Anencephaly Pregnancy, High-Risk Oligohydramnios Polymorphism, Restriction Fragment Length Ultrasonography Agenesis of Corpus Callosum

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