9q22. Medical search. Frequent questions

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Anatomy26

Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 21 Chromosomes, Human Cell Line Isochromosomes Chromosomes, Human, 4-5 Tumor Cells, Cultured COS Cells Cells, Cultured Cell Line, Tumor X Chromosome Chromosomes, Human, X Brain Chromosomes, Human, 19-20 Telomere Cell Membrane

Organisms3

Cricetinae Mice, Transgenic Rhodobacter sphaeroides

Diseases44

Chromosome Deletion Chromosome Aberrations DiGeorge Syndrome Abnormalities, Multiple Chromosome Disorders Genetic Predisposition to Disease Syndrome Chromosome Duplication Monosomy Oligodendroglioma Facies Microcephaly Isochromosomes Myelodysplastic Syndromes Uniparental Disomy Chromosome Fragility Leukemia, Myeloid, Acute Leukemia, Myeloid Williams Syndrome Breast Neoplasms Aneuploidy Leukemia, Lymphocytic, Chronic, B-Cell Brain Neoplasms Lymphoma, B-Cell Leukemia, Myelomonocytic, Acute Lymphoma, B-Cell, Marginal Zone Disease Progression Muscle Hypotonia Heart Defects, Congenital Coloboma Prostatic Neoplasms Anemia, Refractory, with Excess of Blasts Precursor Cell Lymphoblastic Leukemia-Lymphoma Lupus Erythematosus, Systemic Astrocytoma Leukemia Acute Disease Adenocarcinoma Carcinoma, Squamous Cell Cleft Palate Disease Models, Animal Colorectal Neoplasms Leukemia, Monocytic, Acute Cell Transformation, Neoplastic

Chemicals and Drugs54

Complement C1q Ubiquinone GTP-Binding Protein alpha Subunits, Gq-G11 Q beta Replicase Complement Activating Enzymes DNA, Neoplasm Myeloid-Lymphoid Leukemia Protein Glutamine DNA Primers DNA-Binding Proteins DNA, Satellite DNA Transcription Factors DNA, Complementary Coenzymes Neoplasm Proteins RNA, Messenger Recombinant Proteins Phospholipase C beta DNA Probes Nuclear Proteins Carrier Proteins Complement C1r Nerve Tissue Proteins Proteins GTP-Binding Proteins Antigen-Antibody Complex Membrane Proteins Complement C1s Complement C4 Tumor Suppressor Proteins Receptors, Complement GTP-Binding Protein alpha Subunits, G12-G13 Recombinant Fusion Proteins Proto-Oncogene Proteins Aryldialkylphosphatase Mutant Proteins Type C Phospholipases Oncogene Proteins Complement C3 RGS Proteins Arginine Quinones Peptides Calcium RNA, Neoplasm Codon, Nonsense Photosynthetic Reaction Center Complex Proteins Electron Transport Complex III Noble Gases Core Binding Factor Alpha 2 Subunit Homeodomain Proteins Asparagine Tumor Markers, Biological

Analytical, Diagnostic and Therapeutic Techniques and Equipment39

Chromosome Mapping Karyotyping Pedigree Chromosome Banding Comparative Genomic Hybridization Nucleic Acid Hybridization Polymerase Chain Reaction Physical Chromosome Mapping Amino Acid Substitution Genome-Wide Association Study DNA Mutational Analysis Cytogenetic Analysis Mutagenesis, Site-Directed Cloning, Molecular Ventilation-Perfusion Ratio Blotting, Southern Facies Case-Control Studies Models, Molecular Sequence Analysis, DNA Reverse Transcriptase Polymerase Chain Reaction Prognosis Oligonucleotide Array Sequence Analysis Genetic Testing Genetic Association Studies Sequence Alignment Gene Expression Profiling Models, Genetic Artificial Gene Fusion Restriction Mapping Risk Factors Cohort Studies Immunohistochemistry Heterozygote Detection Blotting, Western Blotting, Northern Neoplasm Staging Electrophoresis, Polyacrylamide Gel Disease Models, Animal

Psychiatry and Psychology6

Developmental Disabilities Nuclear Family Family Siblings Autistic Disorder Schizophrenia

Phenomena and Processes107

Chromosome Deletion Chromosomes, Human, Pair 14 Chromosome Aberrations Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 2 Genetic Linkage Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 12 Lod Score Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 18 Microsatellite Repeats Chromosomes, Human, Pair 9 Loss of Heterozygosity Mutation Genetic Predisposition to Disease Base Sequence Amino Acid Sequence Polymorphism, Single Nucleotide Phenotype Genotype Chromosomes, Human, Pair 21 Alleles Gene Dosage Haplotypes Genome, Human Chromosomes, Human Nucleic Acid Hybridization Chromosome Duplication Gene Deletion Genetic Heterogeneity Gene Amplification Amino Acid Substitution Gene Rearrangement Genes, Dominant Mutation, Missense Monosomy Heterozygote Consanguinity Genetic Loci Genes, Recessive Homozygote DNA Copy Number Variations Polymorphism, Genetic Ventilation-Perfusion Ratio Exons Proto-Oncogenes Sequence Homology, Amino Acid Kinetics Complement Pathway, Classical Gene Frequency Allelic Imbalance Point Mutation Linkage Disequilibrium Protein Binding Sequence Deletion Genetic Variation DNA, Satellite Gene Duplication Isochromosomes Binding Sites Chromosomes, Human, 4-5 Protein Structure, Tertiary Chromosome Breakpoints Uniparental Disomy Chromosome Fragility Polymorphism, Single-Stranded Conformational Penetrance Polymorphism, Restriction Fragment Length Multigene Family Gene Expression Cosmids Time Factors Gene Expression Regulation, Neoplastic Mosaicism Signal Transduction Protein Conformation Temperature Aneuploidy Electron Transport Segmental Duplications, Genomic Introns X Chromosome Chromosomes, Human, X Structure-Activity Relationship Oncogenes Recombination, Genetic Protein Structure, Secondary Transcription, Genetic Chromosome Fragile Sites Sequence Homology, Nucleic Acid Oxidation-Reduction Genes Repetitive Sequences, Nucleic Acid Codon, Nonsense Catalysis DNA Methylation Gene Expression Regulation Hydrogen-Ion Concentration Founder Effect Substrate Specificity Chromosomes, Human, 19-20 Inheritance Patterns Telomere

Disciplines and Occupations2

Cytogenetics Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena3

Nuclear Family Family Siblings

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Pharmacopoeias as Topic

Named Groups4

European Continental Ancestry Group Asian Continental Ancestry Group Infant, Newborn Siblings

Health Care7

Genome-Wide Association Study Case-Control Studies Genetic Testing Age of Onset Temperature Risk Factors Cohort Studies

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

Complement C1q Chromosome Mapping Chromosome Deletion Chromosomes, Human, Pair 14 Chromosome Aberrations Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 2 Genetic Linkage Karyotyping Chromosomes, Human, Pair 10 Pedigree Chromosome Banding Chromosomes, Human, Pair 12 Lod Score Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 16 Ubiquinone Chromosomes, Human, Pair 18 Molecular Sequence Data DiGeorge Syndrome Microsatellite Repeats Abnormalities, Multiple Chromosomes, Human, Pair 9 GTP-Binding Protein alpha Subunits, Gq-G11 Chromosome Disorders Loss of Heterozygosity Mutation Genetic Predisposition to Disease Q beta Replicase Base Sequence Amino Acid Sequence Polymorphism, Single Nucleotide Phenotype Complement Activating Enzymes Genotype Syndrome Chromosomes, Human, Pair 21 Alleles Comparative Genomic Hybridization Gene Dosage Haplotypes Genome, Human DNA, Neoplasm Chromosomes, Human Nucleic Acid Hybridization Chromosome Duplication Gene Deletion Polymerase Chain Reaction Physical Chromosome Mapping Genetic Heterogeneity Gene Amplification Amino Acid Substitution Genome-Wide Association Study Gene Rearrangement DNA Mutational Analysis Genes, Dominant Mutation, Missense Cytogenetic Analysis Monosomy Heterozygote Consanguinity Genetic Loci Oligodendroglioma Genes, Recessive Mutagenesis, Site-Directed Cloning, Molecular Homozygote DNA Copy Number Variations Polymorphism, Genetic Ventilation-Perfusion Ratio Myeloid-Lymphoid Leukemia Protein Glutamine Blotting, Southern Cytogenetics Exons Facies Proto-Oncogenes Sequence Homology, Amino Acid Cell Line Kinetics Case-Control Studies Complement Pathway, Classical Gene Frequency DNA Primers Allelic Imbalance Point Mutation Models, Molecular Sequence Analysis, DNA DNA-Binding Proteins Linkage Disequilibrium Protein Binding Sequence Deletion Genetic Variation DNA, Satellite DNA Transcription Factors Gene Duplication Microcephaly

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