Congenital fetal abnormalities. Medical search. Frequent questions

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Anatomy6

Fetus Amniotic Fluid Brain Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 11 Nerve Fibers, Myelinated

Organisms4

Mice, Knockout Mice, Transgenic Mice, Mutant Strains Mice, Inbred C57BL

Diseases35

Congenital Abnormalities Fetal Diseases Polyhydramnios Chromosome Disorders Fetal Death Chromosome Aberrations Pregnancy Complications Abnormalities, Multiple Eye Abnormalities Cardiovascular Abnormalities Craniofacial Abnormalities Syndrome Skin Abnormalities Urogenital Abnormalities Trisomy Musculoskeletal Abnormalities Tooth Abnormalities Translocation, Genetic Aneuploidy Disease Models, Animal Sex Chromosome Aberrations Abnormalities, Drug-Induced 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

Chemicals and Drugs1

alpha-Fetoproteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment28

Prenatal Diagnosis Abortion, Eugenic Ultrasonography, Prenatal Amniocentesis Pregnancy Outcome Karyotyping Magnetic Resonance Imaging In Situ Hybridization, Fluorescence Electrocardiography Disease Models, Animal Retrospective Studies Case-Control Studies Pedigree Prospective Studies Cytogenetic Analysis Tomography, X-Ray Computed Sensitivity and Specificity Chromosome Banding Follow-Up Studies Echocardiography Prognosis Risk Factors Reference Values Biopsy Predictive Value of Tests Electroencephalography Neurologic Examination Diffusion Magnetic Resonance Imaging

Psychiatry and Psychology2

Schizophrenia Intellectual Disability

Phenomena and Processes21

Pregnancy Gestational Age Pregnancy Trimester, Second Pregnancy Trimester, First Pregnancy Outcome Chromosome Aberrations Phenotype Trisomy Mutation Translocation, Genetic Aneuploidy Sex Chromosome Aberrations Time Factors Chromosome Deletion Sensitivity and Specificity Homozygote Heterozygote Chromosomes, Human, Pair 13 Mosaicism Chromosomes, Human, Pair 11 Abnormal Karyotype

Disciplines and Occupations2

Obstetric Nursing Cytogenetics

Information Science1

Image Processing, Computer-Assisted

Named Groups1

Infant, Newborn

Health Care8

Obstetric Nursing Retrospective Studies Case-Control Studies Prospective Studies Sensitivity and Specificity Follow-Up Studies Risk Factors Predictive Value of Tests

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

Congenital Abnormalities Prenatal Diagnosis Abortion, Eugenic Fetal Diseases Ultrasonography, Prenatal Amniocentesis Pregnancy Obstetric Nursing Polyhydramnios Fetus Amniotic Fluid Chromosome Disorders Gestational Age alpha-Fetoproteins Fetal Death Pregnancy Trimester, Second Pregnancy Trimester, First Pregnancy Outcome Chromosome Aberrations Pregnancy Complications Infant, Newborn Abnormalities, Multiple Eye Abnormalities Karyotyping Magnetic Resonance Imaging Brain Cardiovascular Abnormalities Craniofacial Abnormalities Syndrome Skin Abnormalities Phenotype Urogenital Abnormalities Trisomy Mutation Musculoskeletal Abnormalities In Situ Hybridization, Fluorescence Tooth Abnormalities Translocation, Genetic Aneuploidy Electrocardiography Disease Models, Animal Sex Chromosome Aberrations Retrospective Studies Abnormalities, Drug-Induced Case-Control Studies Time Factors Schizophrenia Pedigree Prospective Studies Cytogenetic Analysis Brain Diseases Tomography, X-Ray Computed Mice, Knockout Chromosome Deletion Heart Defects, Congenital Sensitivity and Specificity Image Processing, Computer-Assisted Chromosome Banding Follow-Up Studies Cytogenetics Nervous System Malformations Echocardiography Mice, Transgenic Mice, Mutant Strains Prognosis Homozygote Risk Factors Mice, Inbred C57BL 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 Limb Deformities, Congenital Mosaicism Chromosomes, Human, Pair 11 Neurologic Examination Diffusion Magnetic Resonance Imaging Ocular Motility Disorders Myelodysplastic Syndromes Abnormal Karyotype Nerve Fibers, Myelinated

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