Syndrome aneuploidy. Medical search. Frequent questions

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Anatomy24

Chromosomes, Human, Pair 18 Chromosomes, Human Chromosomes, Human, X Spermatozoa Polar Bodies Chromosomes, Human, Pair 21 Centrosome Chromosomes, Human, Pair 13 Sex Chromosomes Chromosomes, Human, Y Spindle Apparatus Chromosomes Y Chromosome Oocytes X Chromosome Chromatids Chromosomes, Human, Pair 12 Kinetochores Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 17 Centromere Blastomeres Chromosomes, Human, Pair 8 Embryo, Mammalian

Organisms1

Porcine respiratory and reproductive syndrome virus

Diseases59

Aneuploidy Syndrome Down Syndrome Chromosomal Instability Metabolic Syndrome X Chromosome Aberrations Trisomy Chromosome Disorders Nephrotic Syndrome Klinefelter Syndrome Turner Syndrome Abnormal Karyotype Sjogren's Syndrome Polyploidy Abnormalities, Multiple Nondisjunction, Genetic Myelodysplastic Syndromes Sex Chromosome Aberrations Cushing Syndrome Genomic Instability Infertility, Male Acute Coronary Syndrome Polycystic Ovary Syndrome XYY Karyotype Williams Syndrome DiGeorge Syndrome Horner Syndrome Prader-Willi Syndrome Long QT Syndrome Fetal Diseases Oligospermia Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Compartment Syndromes Tourette Syndrome Antiphospholipid Syndrome Abortion, Spontaneous Porcine Reproductive and Respiratory Syndrome Carpal Tunnel Syndrome Werner Syndrome Reye Syndrome Bartter Syndrome HELLP Syndrome Sex Chromosome Disorders Translocation, Genetic Cell Transformation, Neoplastic Tetrasomy Bloom Syndrome Brugada Syndrome Ehlers-Danlos Syndrome Neoplasms Respiratory Distress Syndrome, Adult Angelman Syndrome Severe Acute Respiratory Syndrome Monosomy Restless Legs Syndrome Job Syndrome Wiskott-Aldrich Syndrome Paraneoplastic Syndromes

Chemicals and Drugs9

Aneugens Mad2 Proteins DNA, Neoplasm Aurora Kinases Aurora Kinase A Cell Cycle Proteins p-Fluorophenylalanine Protein-Serine-Threonine Kinases Demecolcine

Analytical, Diagnostic and Therapeutic Techniques and Equipment20

In Situ Hybridization, Fluorescence Karyotyping Preimplantation Diagnosis Prenatal Diagnosis Cytogenetic Analysis Genetic Testing Ultrasonography, Prenatal Primed In Situ Labeling Sperm Injections, Intracytoplasmic Maternal Serum Screening Tests Spectral Karyotyping Amniocentesis Flow Cytometry Pedigree Comparative Genomic Hybridization Nuchal Translucency Measurement Image Cytometry Fertilization in Vitro Risk Factors Chromosome Banding

Psychiatry and Psychology2

Tourette Syndrome Restless Legs Syndrome

Phenomena and Processes48

Aneuploidy Chromosomal Instability Chromosome Aberrations Trisomy Chromosome Segregation Ploidies Mosaicism Chromosomes, Human, Pair 18 Abnormal Karyotype Diploidy Polyploidy Pregnancy Chromosomes, Human Nondisjunction, Genetic Chromosomes, Human, X Meiosis Chromosomes, Human, Pair 21 Karyotype Maternal Age Mitosis Chromosomes, Human, Pair 13 Sex Chromosome Aberrations Sex Chromosomes Chromosomes, Human, Y Genomic Instability Chromosomes Mutation XYY Karyotype Metaphase Y Chromosome Phenotype Pregnancy Trimester, First X Chromosome M Phase Cell Cycle Checkpoints Chromatids Translocation, Genetic Tetrasomy Chromosomes, Human, Pair 12 Kinetochores Gene Dosage Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 17 Centromere Haploidy Heterozygote Monosomy Pregnancy Trimester, Second Chromosomes, Human, Pair 8

Disciplines and Occupations1

Health Care3

Maternal Age Genetic Testing Risk Factors

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Health Care

Aneuploidy Syndrome Down Syndrome Chromosomal Instability In Situ Hybridization, Fluorescence Metabolic Syndrome X Karyotyping Preimplantation Diagnosis Chromosome Aberrations Trisomy Chromosome Segregation Ploidies Chromosome Disorders Mosaicism Nephrotic Syndrome Chromosomes, Human, Pair 18 Klinefelter Syndrome Turner Syndrome Abnormal Karyotype Sjogren's Syndrome Diploidy Polyploidy Abnormalities, Multiple Pregnancy Chromosomes, Human Nondisjunction, Genetic Chromosomes, Human, X Spermatozoa Aneugens Meiosis Polar Bodies Prenatal Diagnosis Chromosomes, Human, Pair 21 Karyotype Maternal Age Centrosome Mitosis Mad2 Proteins Myelodysplastic Syndromes Chromosomes, Human, Pair 13 Sex Chromosome Aberrations Cushing Syndrome Sex Chromosomes Chromosomes, Human, Y Spindle Apparatus Genomic Instability Infertility, Male Acute Coronary Syndrome Polycystic Ovary Syndrome Chromosomes Mutation XYY Karyotype Cytogenetic Analysis Williams Syndrome Metaphase Y Chromosome Phenotype DiGeorge Syndrome Cytogenetics Horner Syndrome Prader-Willi Syndrome DNA, Neoplasm Long QT Syndrome Genetic Testing Ultrasonography, Prenatal Fetal Diseases Primed In Situ Labeling Oligospermia Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Sperm Injections, Intracytoplasmic Aurora Kinases Maternal Serum Screening Tests Spectral Karyotyping Amniocentesis Compartment Syndromes Pregnancy Trimester, First Tourette Syndrome Oocytes Antiphospholipid Syndrome X Chromosome Abortion, Spontaneous Porcine Reproductive and Respiratory Syndrome M Phase Cell Cycle Checkpoints Flow Cytometry Aurora Kinase A Carpal Tunnel Syndrome Werner Syndrome Reye Syndrome Bartter Syndrome Chromatids Porcine respiratory and reproductive syndrome virus Pedigree Cell Cycle Proteins Comparative Genomic Hybridization HELLP Syndrome Sex Chromosome Disorders Translocation, Genetic Cell Transformation, Neoplastic Tetrasomy

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