Genetic disorder trisomy. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy24

Chromosomes, Human, Pair 18 Chromosomes, Human, 16-18 Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 13 Chromosomes, Human, 6-12 and X Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Nasal Bone Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 7 Chromosomes, Human, 19-20 Neck Chromosomes, Human, 4-5 Chromosomes, Human, Pair 22 Chromosomes, Human, 1-3 Fetus Brain Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 15 Forehead Cells, Cultured Chromosomes, Human, Pair 5 Fibroblasts

Diseases52

Trisomy Down Syndrome Genetic Diseases, Inborn Chromosome Disorders Abnormalities, Multiple Chromosome Aberrations Fetal Diseases Syndrome Nondisjunction, Genetic Intellectual Disability Aneuploidy Williams Syndrome Bone Diseases, Developmental Musculoskeletal Abnormalities Prader-Willi Syndrome Translocation, Genetic Metabolism, Inborn Errors Monosomy Turner Syndrome Sex Chromosome Aberrations Disease Models, Animal Iron Metabolism Disorders Substance-Related Disorders Microcephaly Ataxia Telangiectasia Neurofibromatosis 1 Progeria Craniofacial Abnormalities Genetic Predisposition to Disease Pachyonychia Congenita Ectodermal Dysplasia Bloom Syndrome Tuberous Sclerosis Rare Diseases Chondrodysplasia Punctata Chromosome Deletion Myositis Ossificans Tic Disorders Fanconi Anemia Myeloproliferative Disorders Noonan Syndrome Skin Diseases, Genetic Ossification, Heterotopic Cockayne Syndrome Congenital Abnormalities Nervous System Diseases Growth Disorders Hair Diseases Sleep Disorders Facies 22q11 Deletion Syndrome Kallmann Syndrome

Chemicals and Drugs7

Chorionic Gonadotropin, beta Subunit, Human Pregnancy-Associated Plasma Protein-A Neurofibromin 1 Genetic Markers RecQ Helicases Codon, Nonsense DNA

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Karyotyping Prenatal Diagnosis Nuchal Translucency Measurement Ultrasonography, Prenatal Pedigree In Situ Hybridization, Fluorescence Chromosome Banding Dermatoglyphics Amniocentesis Crown-Rump Length Genetic Testing Chorionic Villi Sampling Disease Models, Animal Chromosome Mapping DNA Mutational Analysis Case-Control Studies Preimplantation Diagnosis Risk Factors Polymerase Chain Reaction Cytogenetic Analysis Abortion, Eugenic Facies Prevalence

Psychiatry and Psychology22

Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders Intellectual Disability Depressive Disorder, Major Autistic Disorder Attention Deficit Disorder with Hyperactivity Depressive Disorder Obsessive-Compulsive Disorder Stress Disorders, Post-Traumatic Phobic Disorders Child Development Disorders, Pervasive Psychotic Disorders Substance-Related Disorders Conduct Disorder Tic Disorders Psychiatric Status Rating Scales Borderline Personality Disorder Somatoform Disorders Cognition Disorders Sleep Disorders

Phenomena and Processes50

Trisomy Chromosomes, Human, Pair 18 Chromosomes, Human, 16-18 Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 13 Mosaicism Chromosome Aberrations Pregnancy Mutation Chromosomes, Human, 6-12 and X Chromosomes, Human, 13-15 Nondisjunction, Genetic Pregnancy Trimester, First Maternal Age Phenotype Pregnancy Trimester, Second Chromosomes, Human, 21-22 and Y Aneuploidy Pregnancy, High-Risk Crown-Rump Length Chromosomes, Human, Pair 8 Translocation, Genetic Monosomy Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 7 Chromosomes, Human, 19-20 Genes, Recessive Chromosomes, Human, 4-5 Sex Chromosome Aberrations Heterozygote Chromosomes, Human, Pair 22 Gestational Age Alleles Genetic Predisposition to Disease Chromosomes, Human, 1-3 Genetic Markers Chromosomes, Human, Pair 16 Consanguinity Base Sequence Chromosome Deletion Genotype Chromosomes, Human, Pair 15 Genetic Linkage Mutation, Missense Point Mutation Exons Homozygote Codon, Nonsense Genes, Neurofibromatosis 1 Chromosomes, Human, Pair 5

Disciplines and Occupations3

Genetic Counseling Genetics, Medical Cytogenetics

Anthropology, Education, Sociology and Social Phenomena1

Dermatoglyphics

Humanities1

Information Science4

Diagnostic and Statistical Manual of Mental Disorders Molecular Sequence Data Base Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care8

Maternal Age Genetic Counseling Crown-Rump Length Genetic Testing Genetic Services Case-Control Studies Risk Factors Prevalence

Geographicals1

Mediterranean Islands

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 Geographicals

Trisomy Down Syndrome Genetic Diseases, Inborn Chromosome Disorders Chromosomes, Human, Pair 18 Karyotyping Prenatal Diagnosis Abnormalities, Multiple Chromosomes, Human, 16-18 Bipolar Disorder Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 13 Mosaicism Chromosome Aberrations Mental Disorders Nuchal Translucency Measurement Anxiety Disorders Mood Disorders Pregnancy Chorionic Gonadotropin, beta Subunit, Human Fetal Diseases Mutation Syndrome Chromosomes, Human, 6-12 and X Chromosomes, Human, 13-15 Nondisjunction, Genetic Pregnancy Trimester, First Maternal Age Ultrasonography, Prenatal Pedigree Phenotype Diagnostic and Statistical Manual of Mental Disorders Pregnancy Trimester, Second Pregnancy-Associated Plasma Protein-A Chromosomes, Human, 21-22 and Y Nasal Bone In Situ Hybridization, Fluorescence Genetic Counseling Intellectual Disability Aneuploidy Chromosome Banding Williams Syndrome Dermatoglyphics Pregnancy, High-Risk Depressive Disorder, Major Autistic Disorder Bone Diseases, Developmental Amniocentesis Musculoskeletal Abnormalities Infant, Newborn Attention Deficit Disorder with Hyperactivity Crown-Rump Length Chromosomes, Human, Pair 8 Prader-Willi Syndrome Translocation, Genetic Metabolism, Inborn Errors Depressive Disorder Genetic Testing Monosomy Turner Syndrome Obsessive-Compulsive Disorder Stress Disorders, Post-Traumatic Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 7 Chromosomes, Human, 19-20 Genes, Recessive Neck Chorionic Villi Sampling Chromosomes, Human, 4-5 Sex Chromosome Aberrations Disease Models, Animal Phobic Disorders Heterozygote Child Development Disorders, Pervasive Iron Metabolism Disorders Psychotic Disorders Substance-Related Disorders Genetic Services Mediterranean Islands Chromosomes, Human, Pair 22 Gestational Age Chromosome Mapping Microcephaly Ataxia Telangiectasia Neurofibromin 1 Neurofibromatosis 1 Molecular Sequence Data Alleles Progeria Craniofacial Abnormalities Eugenics Genetic Predisposition to Disease Pachyonychia Congenita Ectodermal Dysplasia Bloom Syndrome Tuberous Sclerosis Chromosomes, Human, 1-3 Conduct Disorder Genetic Markers Fetus

No FAQ available that match "genetic disorder trisomy"