Growth retardation prenatal diagnosis. Medical search. Frequent questions

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Anatomy23

Amniotic Fluid Fetus Placenta Chromosomes, Human, Pair 18 X Chromosome Fetal Heart Chorionic Villi Fetal Blood Umbilical Arteries Chromosomes, Human, Pair 13 Chromosomes, Human, X Growth Plate Chromosomes, Human, Pair 21 Brain Arm Bones Face Embryo, Mammalian Chromosomes, Human, Pair 22 Cloaca Umbilical Cord Liver Azygos Vein Trophoblasts

Organisms4

Mice, Knockout Mice, Inbred C57BL Animals, Newborn Mice, Mutant Strains

Diseases109

Fetal Growth Retardation Fetal Diseases Growth Disorders Prenatal Exposure Delayed Effects Abnormalities, Multiple Intellectual Disability Syndrome Fetal Death Mental Retardation, X-Linked Chromosome Disorders Trisomy Microcephaly Congenital Abnormalities Down Syndrome Thalassemia Heart Defects, Congenital Chromosome Aberrations Hydrops Fetalis Pregnancy Complications Sex Chromosome Aberrations Sex Chromosome Disorders Birth Weight Facies Polyhydramnios Hemoglobinopathies Dwarfism Fragile X Syndrome Oligohydramnios Ectromelia Genetic Diseases, Inborn Hernia, Umbilical Fetal Weight Abnormalities, Drug-Induced beta-Thalassemia Aneuploidy Twins, Conjoined Bone Diseases, Developmental Micrognathism Prenatal Injuries Musculoskeletal Abnormalities Chromosome Deletion Neural Tube Defects Body Weight Hydrocolpos Dandy-Walker Syndrome Skin Abnormalities Anus, Imperforate Foot Deformities, Congenital Agenesis of Corpus Callosum Failure to Thrive Levocardia Gastroschisis Pulmonary Atresia Muscular Dystrophies Fetomaternal Transfusion Adrenal Hyperplasia, Congenital Fetal Alcohol Spectrum Disorders Hernia, Diaphragmatic Spinal Muscular Atrophies of Childhood Placenta Diseases Anencephaly Hand Deformities, Congenital alpha-Thalassemia Nutrition Disorders Turner Syndrome Toxoplasmosis, Congenital Cystic Adenomatoid Malformation of Lung, Congenital Psychomotor Disorders Spinal Dysraphism Osteochondrodysplasias Hypoplastic Left Heart Syndrome Hydronephrosis Amniotic Band Syndrome Obstetric Labor, Premature Translocation, Genetic Metabolism, Inborn Errors Encephalocele Cleft Palate Amino Acid Metabolism, Inborn Errors Meningomyelocele Urogenital Abnormalities Pregnancy Complications, Infectious Abortion, Spontaneous Intestinal Atresia Rare Diseases Fetal Hypoxia Cri-du-Chat Syndrome Disease Models, Animal Hydrocephalus Heart Septal Defects Citrullinemia Embryo Loss Respiratory System Abnormalities Lymphangioma, Cystic Meningocele Craniofacial Abnormalities Placental Insufficiency Hemophilia A Ornithine Carbamoyltransferase Deficiency Disease Holoprosencephaly Blepharophimosis Weight Gain Fetal Resorption Pre-Eclampsia Cystic Fibrosis Spina Bifida Occulta Hypophosphatasia XYY Karyotype Lymphangioma

Chemicals and Drugs12

Fragile X Mental Retardation Protein DNA Genetic Markers Teratogens Growth Hormone Insulin-Like Growth Factor I Steroid 21-Hydroxylase DNA Primers RNA, Messenger Globins Codon, Nonsense DNA Probes

Analytical, Diagnostic and Therapeutic Techniques and Equipment62

Prenatal Diagnosis Ultrasonography, Prenatal Chorionic Villi Sampling Prenatal Care Amniocentesis Abortion, Eugenic Heterozygote Detection Abortion, Therapeutic Pregnancy Outcome Cordocentesis Karyotyping Pedigree Abortion, Induced Genetic Testing Sensitivity and Specificity Birth Weight Facies Retrospective Studies Polymerase Chain Reaction Ultrasonography, Doppler, Color Fatal Outcome Preimplantation Diagnosis Fetal Weight Sex Determination Analysis In Situ Hybridization, Fluorescence Body Height Delayed Diagnosis DNA Mutational Analysis Fetoscopy Body Weight Ultrasonography Ultrasonography, Doppler, Pulsed Early Diagnosis Prospective Studies Magnetic Resonance Imaging Risk Factors Echocardiography, Four-Dimensional Follow-Up Studies Chromosome Banding Organ Size Reproducibility of Results Cohort Studies Gene Targeting Age Determination by Skeleton Diagnosis Abortion, Legal Cesarean Section Diagnostic Errors Predictive Value of Tests Prevalence Chromosome Mapping Imaging, Three-Dimensional Crown-Rump Length Disease Models, Animal Prognosis Neonatal Screening Biopsy Anthropometry Ultrasonography, Doppler Case-Control Studies Treatment Outcome Nuchal Translucency Measurement

Psychiatry and Psychology6

Intellectual Disability Developmental Disabilities Mothers Psychomotor Disorders Child Development Maternal-Fetal Relations

Phenomena and Processes56

Pregnancy Gestational Age Pregnancy Trimester, Second Pregnancy Outcome Trisomy Pregnancy Trimester, First Pregnancy Trimester, Third Growth Chromosome Aberrations Sex Chromosome Aberrations Sensitivity and Specificity Mutation Birth Weight Phenotype Mosaicism Maternal-Fetal Exchange Consanguinity Chromosomes, Human, Pair 18 Embryonic and Fetal Development Fetal Weight Genes, Recessive X Chromosome Fetal Development Heterozygote Genetic Linkage Aneuploidy Body Height Base Sequence Maternal Age Homozygote Chromosome Deletion Body Weight Chromosomes, Human, Pair 13 Genetic Markers Time Factors Chromosomes, Human, X Pregnancy, High-Risk Polymorphism, Restriction Fragment Length Chromosomes, Human, Pair 21 Alleles Organ Size Genotype Gene Deletion Genomic Imprinting Translocation, Genetic Child Development Placental Circulation Karyotype Chromosomes, Human, Pair 22 Crown-Rump Length Exons Litter Size Bone Development Weight Gain Codon, Nonsense XYY Karyotype

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Mothers Ethnology

Information Science5

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

Named Groups7

Infant, Newborn Pregnant Women Infant, Small for Gestational Age Infant, Low Birth Weight Mothers Infant, Premature Infant, Postmature

Health Care22

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

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 Information Science Named Groups Health Care

Prenatal Diagnosis Fetal Growth Retardation Fetal Diseases Pregnancy Ultrasonography, Prenatal Growth Disorders Prenatal Exposure Delayed Effects Chorionic Villi Sampling Prenatal Care Amniocentesis Abnormalities, Multiple Abortion, Eugenic Intellectual Disability Infant, Newborn Gestational Age Heterozygote Detection Genetic Counseling Amniotic Fluid Syndrome Fetal Death Abortion, Therapeutic Pregnancy Trimester, Second Fetus Pregnancy Outcome Mental Retardation, X-Linked Cordocentesis Chromosome Disorders Trisomy Karyotyping Pedigree Abortion, Induced Microcephaly Fragile X Mental Retardation Protein Congenital Abnormalities Pregnancy Trimester, First Down Syndrome Thalassemia Genetic Testing Pregnancy Trimester, Third Growth Heart Defects, Congenital Chromosome Aberrations Hydrops Fetalis Pregnancy Complications Sex Chromosome Aberrations Sex Chromosome Disorders Placenta Sensitivity and Specificity Mutation Birth Weight Facies Phenotype Polyhydramnios Hemoglobinopathies Retrospective Studies Polymerase Chain Reaction Dwarfism Fragile X Syndrome Ultrasonography, Doppler, Color Oligohydramnios Mosaicism Maternal-Fetal Exchange Ectromelia Consanguinity Fatal Outcome Chromosomes, Human, Pair 18 Preimplantation Diagnosis Genetic Diseases, Inborn Hernia, Umbilical Embryonic and Fetal Development Fetal Weight Pregnant Women Abnormalities, Drug-Induced beta-Thalassemia Sex Determination Analysis Genes, Recessive X Chromosome Fetal Development Heterozygote Fetal Heart Chorionic Villi Genetic Linkage Aneuploidy Twins, Conjoined In Situ Hybridization, Fluorescence Bone Diseases, Developmental Micrognathism DNA Body Height Base Sequence Delayed Diagnosis Infant, Small for Gestational Age Maternal Age Maternal Exposure DNA Mutational Analysis Infant, Low Birth Weight Homozygote Prenatal Injuries Molecular Sequence Data Musculoskeletal Abnormalities

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