Genet prenatal diagnosis. Medical search. Frequent questions

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Anatomy18

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

Organisms2

Sasa Escherichia coli

Diseases112

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

Chemicals and Drugs10

Genetic Markers DNA Steroid 21-Hydroxylase Globins 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine DNA Primers DNA Probes DNA Restriction Enzymes alpha-Fetoproteins alpha-Globins

Analytical, Diagnostic and Therapeutic Techniques and Equipment62

Prenatal Diagnosis Ultrasonography, Prenatal Chorionic Villi Sampling Prenatal Care Amniocentesis Abortion, Eugenic Heterozygote Detection Abortion, Therapeutic Abortion, Induced Pregnancy Outcome Genetic Testing Karyotyping Sensitivity and Specificity Pedigree Polymerase Chain Reaction Preimplantation Diagnosis Ultrasonography, Doppler, Color Retrospective Studies Sex Determination Analysis Delayed Diagnosis Fetoscopy Fatal Outcome Early Diagnosis Echocardiography, Four-Dimensional Magnetic Resonance Imaging DNA Mutational Analysis Prospective Studies Diagnosis Reproducibility of Results Abortion, Legal Diagnostic Errors Risk Factors Imaging, Three-Dimensional Ultrasonography, Doppler, Pulsed In Situ Hybridization, Fluorescence Chromosome Mapping Ultrasonography Predictive Value of Tests Follow-Up Studies Biopsy Neonatal Screening Cohort Studies Nuchal Translucency Measurement Prognosis Prevalence Echoencephalography Clinical Enzyme Tests Autopsy Postnatal Care Sequence Analysis, DNA False Positive Reactions Cloning, Molecular Tomography, X-Ray Computed Questionnaires Incidence Treatment Outcome Echocardiography Diagnosis, Computer-Assisted False Negative Reactions Restriction Mapping Birth Weight Ultrasonography, Doppler

Psychiatry and Psychology4

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

Phenomena and Processes47

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

Disciplines and Occupations2

Genetic Counseling Perinatology

Anthropology, Education, Sociology and Social Phenomena2

Mothers Autopsy

Humanities2

Postmodernism Ethics, Medical

Information Science10

Molecular Sequence Data Base Sequence Fatal Outcome Imaging, Three-Dimensional International Classification of Diseases Amino Acid Sequence Prevalence Questionnaires Incidence Diagnosis, Computer-Assisted

Named Groups5

Infant, Newborn Pregnant Women Mothers Triplets Arabs

Health Care24

Prenatal Care Genetic Counseling Genetic Testing Sensitivity and Specificity Retrospective Studies Fatal Outcome Maternal Age Genetic Services Maternal Exposure Prospective Studies Reproducibility of Results Diagnostic Errors Risk Factors Predictive Value of Tests Follow-Up Studies Neonatal Screening Cohort Studies Prevalence Postnatal Care Questionnaires Incidence Treatment Outcome Ethics, Medical Nursing Diagnosis

Geographicals2

Israel United States

Anatomy Organisms 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 Abortion, Therapeutic Infant, Newborn Amniotic Fluid Gestational Age Pregnancy Trimester, Second Abnormalities, Multiple Abortion, Induced Fetus Pregnancy Outcome Chromosome Disorders Thalassemia Trisomy Back Pain Genetic Testing Pregnancy Trimester, First Down Syndrome Hydrops Fetalis Karyotyping Fetal Death Sex Chromosome Disorders Sensitivity and Specificity Hemoglobinopathies Polyhydramnios Congenital Abnormalities Heart Defects, Congenital Pedigree Pregnancy Trimester, Third Polymerase Chain Reaction Preimplantation Diagnosis Genetic Linkage Ectromelia Ultrasonography, Doppler, Color Hernia, Umbilical Retrospective Studies Mutation Pregnant Women beta-Thalassemia Sex Determination Analysis Fetal Heart Syndrome Chorionic Villi Genetic Diseases, Inborn Sex Chromosome Aberrations Twins, Conjoined Aneuploidy Chromosome Aberrations Molecular Sequence Data Genetic Markers Delayed Diagnosis Base Sequence Prenatal Injuries Fetoscopy Chromosomes, Human, Pair 18 Fatal Outcome Hydrocolpos Early Diagnosis Dandy-Walker Syndrome Musculoskeletal Abnormalities DNA Levocardia Gastroschisis Mosaicism Pulmonary Atresia Chromosomes, Human, Pair 13 Fetomaternal Transfusion Adrenal Hyperplasia, Congenital Maternal Age Genetic Services Anus, Imperforate Echocardiography, Four-Dimensional Muscular Dystrophies Sasa Hernia, Diaphragmatic Spinal Muscular Atrophies of Childhood Alleles Anencephaly Oligohydramnios Pregnancy, High-Risk Agenesis of Corpus Callosum Magnetic Resonance Imaging DNA Mutational Analysis Genotype Polymorphism, Restriction Fragment Length Maternal Exposure Neural Tube Defects Prospective Studies Cystic Adenomatoid Malformation of Lung, Congenital Spinal Dysraphism Phenotype

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