Challenge down syndrome. Medical search. Frequent questions

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Anatomy5

Chromosomes, Human, Pair 21 Chromosomes, Human, 21-22 and Y Nasal Bone Brain Neck

Organisms1

Mice, Inbred C57BL

Diseases36

Down Syndrome Syndrome Trisomy Metabolic Syndrome X Leukemia, Megakaryoblastic, Acute Fetal Diseases Nephrotic Syndrome Sjogren's Syndrome Intellectual Disability Turner Syndrome Abnormalities, Multiple Disease Models, Animal Nondisjunction, Genetic Williams Syndrome Myelodysplastic Syndromes Cushing Syndrome Heart Defects, Congenital Acute Coronary Syndrome Polycystic Ovary Syndrome Chromosome Disorders DiGeorge Syndrome Horner Syndrome Long QT Syndrome Craniofacial Abnormalities Prader-Willi Syndrome Heart Septal Defects Alzheimer Disease Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Duodenal Obstruction Compartment Syndromes Tourette Syndrome Porcine Reproductive and Respiratory Syndrome Antiphospholipid Syndrome Klinefelter Syndrome Chromosome Aberrations

Chemicals and Drugs7

Estriol alpha-Fetoproteins Pregnancy-Associated Plasma Protein-A Chorionic Gonadotropin, beta Subunit, Human Biological Markers GATA1 Transcription Factor Chorionic Gonadotropin

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Prenatal Diagnosis Amniocentesis Abortion, Eugenic Karyotyping Disease Models, Animal Nuchal Translucency Measurement Ultrasonography, Prenatal False Positive Reactions Case-Control Studies Risk Factors Genetic Testing Retrospective Studies Prevalence Pedigree Treatment Outcome

Psychiatry and Psychology4

Intellectual Disability Stanford-Binet Test Alzheimer Disease Tourette Syndrome

Phenomena and Processes16

Chromosomes, Human, Pair 21 Trisomy Maternal Age Pregnancy Trimester, Second Pregnancy Chromosomes, Human, 21-22 and Y Nondisjunction, Genetic Pregnancy, High-Risk Pregnancy Trimester, First Phenotype Paternal Age Time Factors Mutation Gestational Age Mosaicism Chromosome Aberrations

Information Science2

Prevalence Molecular Sequence Data

Named Groups1

Infant, Newborn

Health Care7

Maternal Age Case-Control Studies Risk Factors Genetic Testing Retrospective Studies Prevalence Treatment Outcome

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care

Down Syndrome Syndrome Chromosomes, Human, Pair 21 Prenatal Diagnosis Trisomy Maternal Age Metabolic Syndrome X Estriol Pregnancy Trimester, Second Pregnancy Amniocentesis Leukemia, Megakaryoblastic, Acute Fetal Diseases Chromosomes, Human, 21-22 and Y Nephrotic Syndrome Abortion, Eugenic Sjogren's Syndrome Intellectual Disability Infant, Newborn Turner Syndrome Karyotyping Abnormalities, Multiple alpha-Fetoproteins Nasal Bone Disease Models, Animal Nuchal Translucency Measurement Nondisjunction, Genetic Ultrasonography, Prenatal Pregnancy, High-Risk Pregnancy Trimester, First Williams Syndrome Phenotype Myelodysplastic Syndromes Pregnancy-Associated Plasma Protein-A Chorionic Gonadotropin, beta Subunit, Human Cushing Syndrome False Positive Reactions Heart Defects, Congenital Paternal Age Acute Coronary Syndrome Polycystic Ovary Syndrome Chromosome Disorders Case-Control Studies Risk Factors Time Factors Mutation DiGeorge Syndrome Horner Syndrome Long QT Syndrome Craniofacial Abnormalities Prader-Willi Syndrome Brain Stanford-Binet Test Biological Markers Genetic Testing Heart Septal Defects Alzheimer Disease Retrospective Studies Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Duodenal Obstruction Prevalence Compartment Syndromes GATA1 Transcription Factor Tourette Syndrome Chorionic Gonadotropin Porcine Reproductive and Respiratory Syndrome Pedigree Antiphospholipid Syndrome Gestational Age Mosaicism Treatment Outcome Mice, Inbred C57BL Klinefelter Syndrome Molecular Sequence Data Neck Chromosome Aberrations

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