Prenatal diagnosis mosaicism. Medical search. Frequent questions

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Anatomy22

Amniotic Fluid Fetus Chromosomes, Human, Pair 18 Chorionic Villi X Chromosome Chromosomes, Human, X Chromosomes, Human, Pair 13 Fetal Heart Chromosomes, Human, Pair 21 Y Chromosome Chromosomes, Human, Y Sex Chromosomes Fetal Blood Ring Chromosomes Chromosomes, Human, Pair 22 Placenta Cloaca Umbilical Cord Chromosomes, Human, 21-22 and Y Azygos Vein Chromosomes, Human, 13-15 Sacrococcygeal Region

Diseases97

Fetal Diseases Prenatal Exposure Delayed Effects Trisomy Sex Chromosome Aberrations Abnormalities, Multiple Chromosome Disorders Turner Syndrome Down Syndrome Aneuploidy Chromosome Aberrations Sex Chromosome Disorders Thalassemia Gonadal Dysgenesis, Mixed Syndrome Hydrops Fetalis Fetal Death Heart Defects, Congenital Hemoglobinopathies Polyhydramnios Congenital Abnormalities Genetic Diseases, Inborn Epidermolysis Bullosa Ectromelia Hernia, Umbilical beta-Thalassemia Klinefelter Syndrome Twins, Conjoined Pigmentation Disorders Uniparental Disomy Prenatal Injuries Hydrocolpos Muscular Dystrophies Intellectual Disability Hernia, Diaphragmatic Cryopyrin-Associated Periodic Syndromes Dandy-Walker Syndrome Musculoskeletal Abnormalities Levocardia Gastroschisis Pulmonary Atresia XYY Karyotype Fetomaternal Transfusion Adrenal Hyperplasia, Congenital Anus, Imperforate Chromosome Deletion Foot Deformities, Congenital Spinal Muscular Atrophies of Childhood Anencephaly Oligohydramnios Agenesis of Corpus Callosum Chondrodysplasia Punctata Neurofibromatosis 2 Neural Tube Defects Cystic Adenomatoid Malformation of Lung, Congenital Spinal Dysraphism Hypoplastic Left Heart Syndrome Pregnancy Complications Ring Chromosomes Hydronephrosis Micrognathism Amniotic Band Syndrome Toxoplasmosis, Congenital Encephalocele Meningomyelocele Bone Diseases, Developmental Intestinal Atresia Translocation, Genetic Abortion, Spontaneous Heart Septal Defects Citrullinemia Gonadal Dysgenesis Respiratory System Abnormalities alpha-Thalassemia Diseases in Twins 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 Myotonic Dystrophy Hypophosphatasia Lymphangioma Fragile X Syndrome Prader-Willi Syndrome Chromosome Inversion Hydrocephalus Tricuspid Atresia Cri-du-Chat Syndrome Clubfoot Klippel-Trenaunay-Weber Syndrome Bronchopulmonary Sequestration

Chemicals and Drugs5

DNA Genetic Markers Steroid 21-Hydroxylase DNA Probes Globins

Analytical, Diagnostic and Therapeutic Techniques and Equipment51

Prenatal Diagnosis Ultrasonography, Prenatal Chorionic Villi Sampling Amniocentesis Prenatal Care Abortion, Eugenic Heterozygote Detection Karyotyping Abortion, Therapeutic Pedigree Abortion, Induced Pregnancy Outcome Genetic Testing Preimplantation Diagnosis Cordocentesis Sensitivity and Specificity Polymerase Chain Reaction In Situ Hybridization, Fluorescence Sex Determination Analysis Retrospective Studies Ultrasonography, Doppler, Color DNA Mutational Analysis Fatal Outcome Delayed Diagnosis Fetoscopy Early Diagnosis Chromosome Banding Echocardiography, Four-Dimensional Magnetic Resonance Imaging Reproducibility of Results Prospective Studies Diagnosis Risk Factors Abortion, Legal Diagnostic Errors Imaging, Three-Dimensional Ultrasonography, Doppler, Pulsed Comparative Genomic Hybridization Ultrasonography Predictive Value of Tests Follow-Up Studies Biopsy Neonatal Screening Cohort Studies Nuchal Translucency Measurement Prognosis Prevalence Sequence Analysis, DNA Echoencephalography Cesarean Section Clinical Enzyme Tests

Psychiatry and Psychology3

Intellectual Disability Mothers Maternal-Fetal Relations

Phenomena and Processes52

Mosaicism Pregnancy Trisomy Sex Chromosome Aberrations Gestational Age Pregnancy Trimester, Second Aneuploidy Pregnancy Outcome Chromosome Aberrations Pregnancy Trimester, First Sensitivity and Specificity Chromosomes, Human, Pair 18 X Chromosome Chromosomes, Human, X Pregnancy Trimester, Third Chromosomes, Human, Pair 13 Mutation Genetic Linkage Heterozygote Genetic Markers Uniparental Disomy Maternal Age Chromosomes, Human, Pair 21 Phenotype Karyotype Alleles Polymorphism, Restriction Fragment Length Y Chromosome XYY Karyotype Chromosome Deletion Chromosomes, Human, Y Pregnancy, High-Risk Genes, Recessive Sex Chromosomes Base Sequence Ring Chromosomes Maternal-Fetal Exchange Chromosomes, Human, Pair 22 Genotype Exons Consanguinity Germ-Line Mutation Translocation, Genetic Time Factors Homozygote Chromosomes, Human, 21-22 and Y Polymorphism, Genetic Chromosome Inversion Tandem Repeat Sequences Haplotypes Chromosomes, Human, 13-15 Pregnancy Trimesters

Disciplines and Occupations2

Genetic Counseling Perinatology

Anthropology, Education, Sociology and Social Phenomena1

Humanities1

Information Science5

Fatal Outcome Base Sequence Imaging, Three-Dimensional Molecular Sequence Data Prevalence

Named Groups3

Infant, Newborn Pregnant Women Mothers

Health Care18

Prenatal Care Genetic Counseling Genetic Testing Sensitivity and Specificity Retrospective Studies Fatal Outcome Maternal Age Genetic Services Reproducibility of Results Maternal Exposure Prospective Studies Risk Factors Diagnostic Errors Predictive Value of Tests Follow-Up Studies Neonatal Screening Cohort Studies Prevalence

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

Mosaicism Prenatal Diagnosis Fetal Diseases Pregnancy Ultrasonography, Prenatal Chorionic Villi Sampling Prenatal Exposure Delayed Effects Amniocentesis Prenatal Care Abortion, Eugenic Genetic Counseling Trisomy Heterozygote Detection Sex Chromosome Aberrations Karyotyping Abnormalities, Multiple Infant, Newborn Chromosome Disorders Amniotic Fluid Abortion, Therapeutic Gestational Age Pregnancy Trimester, Second Turner Syndrome Pedigree Fetus Abortion, Induced Down Syndrome Aneuploidy Pregnancy Outcome Chromosome Aberrations Genetic Testing Preimplantation Diagnosis Sex Chromosome Disorders Thalassemia Cordocentesis Gonadal Dysgenesis, Mixed Syndrome Pregnancy Trimester, First Hydrops Fetalis Fetal Death Sensitivity and Specificity Heart Defects, Congenital Polymerase Chain Reaction In Situ Hybridization, Fluorescence Chromosomes, Human, Pair 18 Hemoglobinopathies Sex Determination Analysis Polyhydramnios Chorionic Villi X Chromosome Congenital Abnormalities Chromosomes, Human, X Pregnancy Trimester, Third Genetic Diseases, Inborn Retrospective Studies Epidermolysis Bullosa Ectromelia Ultrasonography, Doppler, Color Hernia, Umbilical Chromosomes, Human, Pair 13 DNA Mutational Analysis Pregnant Women beta-Thalassemia Fetal Heart Mutation Klinefelter Syndrome Fatal Outcome Twins, Conjoined Pigmentation Disorders Genetic Linkage Heterozygote DNA Genetic Markers Uniparental Disomy Maternal Age Delayed Diagnosis Prenatal Injuries Fetoscopy Chromosomes, Human, Pair 21 Hydrocolpos Muscular Dystrophies Intellectual Disability Phenotype Early Diagnosis Hernia, Diaphragmatic Cryopyrin-Associated Periodic Syndromes Karyotype Dandy-Walker Syndrome Musculoskeletal Abnormalities Alleles Chromosome Banding Polymorphism, Restriction Fragment Length Y Chromosome Levocardia Gastroschisis Pulmonary Atresia XYY Karyotype Fetomaternal Transfusion Adrenal Hyperplasia, Congenital Genetic Services

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