16p11 2 deletion syndrome chromosome deletion. Medical search. Frequent questions

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Anatomy56

Chromosomes, Human, Pair 22 Y Chromosome Chromosomes Chromosomes, Human, Y Chromosomes, Human, Pair 1 X Chromosome Chromosomes, Human, Pair 6 Sex Chromosomes Chromosomes, Human Chromosomes, Human, Pair 7 Chromosomes, Bacterial Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 17 Parietal Bone Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 13 Chromosomes, Fungal Chromosomes, Human, 6-12 and X Chromosomes, Plant Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 8 Chromosomes, Mammalian Chromosomes, Human, X Chromosomes, Artificial, Bacterial Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 12 Chromosomes, Human, 1-3 Chromosomes, Human, Pair 14 Chromosomes, Artificial, Yeast Chromosomes, Human, Pair 20 Chromosomes, Human, 16-18 Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Ring Chromosomes Chromosomes, Human, 4-5 Branchial Region Brain Centromere Hybrid Cells Cell Line Chromosomes, Insect Chromosomes, Human, 19-20 Chromosome Structures Telomere Kinetochores Cells, Cultured Chromosomes, Artificial, Human Cell Nucleus Spindle Apparatus

Organisms6

Staphylococcus lugdunensis Mice, Inbred C57BL Escherichia coli Saccharomyces cerevisiae Mice, Knockout Drosophila melanogaster

Diseases55

22q11 Deletion Syndrome Chromosome Deletion DiGeorge Syndrome Syndrome Sex Chromosome Disorders of Sex Development Oligospermia Velopharyngeal Insufficiency Sex Chromosome Aberrations Chromosome Aberrations Abnormalities, Multiple Chromosome Disorders Infertility, Male Craniofacial Abnormalities Intellectual Disability Jacobsen Distal 11q Deletion Syndrome Chromosome Breakage Hypoparathyroidism Cri-du-Chat Syndrome Facies WAGR Syndrome Hypocalcemia Muscle Hypotonia Translocation, Genetic Heart Defects, Congenital Eye Abnormalities Monosomy Down Syndrome Exostoses, Multiple Hereditary Learning Disorders Chromosome Inversion Metabolic Syndrome X Language Development Disorders Ring Chromosomes Cleft Palate Genetic Predisposition to Disease Growth Disorders Turner Syndrome Nephrotic Syndrome Aneuploidy Prader-Willi Syndrome Sjogren's Syndrome Williams Syndrome Seizures Trisomy Myelodysplastic Syndromes Angelman Syndrome Nondisjunction, Genetic Klinefelter Syndrome Chromosome Fragility Chromosome Duplication Chromosomal Instability Cushing Syndrome Polycystic Ovary Syndrome Acute Coronary Syndrome Long QT Syndrome

Chemicals and Drugs25

Catechol O-Methyltransferase T-Box Domain Proteins Genetic Markers DNA DNA-Binding Proteins DNA Primers Nuclear Proteins Transcription Factors Bacterial Proteins RNA, Messenger DNA Probes DNA Transposable Elements Saccharomyces cerevisiae Proteins DNA, Bacterial Chromosomal Proteins, Non-Histone Cell Cycle Proteins DNA, Satellite DNA Restriction Enzymes Fungal Proteins Recombinant Fusion Proteins Carrier Proteins Membrane Proteins DNA, Complementary DNA, Fungal DNA, Neoplasm

Analytical, Diagnostic and Therapeutic Techniques and Equipment28

Chromosome Mapping Karyotyping In Situ Hybridization, Fluorescence Chromosome Banding Facies Pedigree Comparative Genomic Hybridization Chromosome Painting Cloning, Molecular Polymerase Chain Reaction DNA Mutational Analysis Sequence Analysis, DNA Blotting, Southern Case-Control Studies Crosses, Genetic Magnetic Resonance Imaging Genetic Association Studies Nucleic Acid Hybridization Models, Genetic Genetic Complementation Test Sequence Alignment Analysis of Variance Mutagenesis, Insertional Chromosome Walking Cytogenetic Analysis Transfection Restriction Mapping Genetic Testing

Psychiatry and Psychology13

Intellectual Disability Developmental Disabilities Schizophrenia Stanford-Binet Test Learning Disorders Intelligence Tests Siblings Cognition Disorders Intelligence Neuropsychological Tests Psychotic Disorders Psychiatric Status Rating Scales Mental Disorders

Phenomena and Processes136

Chromosome Deletion Chromosomes, Human, Pair 22 Y Chromosome Gene Deletion Sex Chromosome Aberrations Chromosome Aberrations Chromosomes Chromosomes, Human, Y Sequence Deletion Sequence Tagged Sites Phenotype Chromosomes, Human, Pair 1 X Chromosome Chromosome Breakage Chromosomes, Human, Pair 6 Sex Chromosomes Mutation Chromosomes, Human Base Sequence Chromosomes, Human, Pair 7 Chromosomes, Bacterial Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 17 Hemizygote Chromosome Segregation Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 13 Chromosomes, Fungal Chromosomes, Human, 6-12 and X Chromosomes, Plant Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 5 Translocation, Genetic Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 8 Chromosomes, Mammalian Chromosomes, Human, X Chromosome Pairing Chromosomes, Artificial, Bacterial Chromosomes, Human, Pair 19 Monosomy Chromosomes, Human, Pair 12 Chromosomes, Human, 1-3 Genotype Amino Acid Sequence Genetic Linkage Chromosomes, Human, Pair 14 Chromosomes, Artificial, Yeast Chromosomes, Human, Pair 20 Genetic Markers Gene Dosage Chromosomes, Human, 16-18 Chromosomes, Human, 13-15 Chromosome Inversion Gene Rearrangement Chromosomes, Human, 21-22 and Y Ring Chromosomes Recombination, Genetic Alleles Chromosomes, Human, 4-5 Chromosome Positioning X Chromosome Inactivation Centromere Plasmids Genetic Predisposition to Disease Exons Microsatellite Repeats Polymorphism, Single Nucleotide Meiosis Heterozygote Homozygote Aneuploidy Mitosis Chromosomes, Insect Transcription, Genetic Chromosomes, Human, 19-20 Chromosome Structures Metaphase Nucleic Acid Hybridization Repetitive Sequences, Nucleic Acid Genes Lod Score Promoter Regions, Genetic Trisomy Polymorphism, Genetic Sequence Homology, Amino Acid Haplotypes Multigene Family Genes, Bacterial Telomere Mosaicism DNA Transposable Elements Genetic Variation Loss of Heterozygosity Mutagenesis Sequence Homology, Nucleic Acid Evolution, Molecular Genes, Recessive DNA Replication Mutagenesis, Insertional Gene Expression Regulation Clonal Deletion Nondisjunction, Genetic Chromosome Fragility Frameshift Mutation Chromosome Duplication Point Mutation Polymorphism, Restriction Fragment Length Chromosomal Instability Protein Structure, Tertiary Genes, Dominant Protein Binding Kinetochores Gene Duplication Genes, Fungal Genome, Human DNA, Satellite Introns Chromosome Breakpoints Chromosomes, Artificial, Human Binding Sites Transfection Cosmids Species Specificity Genes, Lethal Diploidy Phylogeny Gene Expression Quantitative Trait Loci Genes, Tumor Suppressor Genetic Loci

Disciplines and Occupations1

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny

Named Groups2

Infant, Newborn Siblings

Health Care3

Case-Control Studies Analysis of Variance Genetic Testing

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

22q11 Deletion Syndrome Chromosome Deletion Chromosomes, Human, Pair 22 DiGeorge Syndrome Y Chromosome Syndrome Gene Deletion Chromosome Mapping Sex Chromosome Disorders of Sex Development Oligospermia Velopharyngeal Insufficiency Sex Chromosome Aberrations Karyotyping Chromosome Aberrations Chromosomes Chromosomes, Human, Y Sequence Deletion In Situ Hybridization, Fluorescence Sequence Tagged Sites Abnormalities, Multiple Chromosome Disorders Infertility, Male Phenotype Craniofacial Abnormalities Chromosome Banding Chromosomes, Human, Pair 1 Intellectual Disability X Chromosome Jacobsen Distal 11q Deletion Syndrome Chromosome Breakage Chromosomes, Human, Pair 6 Molecular Sequence Data Sex Chromosomes Hypoparathyroidism Developmental Disabilities Mutation Chromosomes, Human Base Sequence Cri-du-Chat Syndrome Chromosomes, Human, Pair 7 Chromosomes, Bacterial Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 17 Parietal Bone Hemizygote Chromosome Segregation Chromosomes, Human, Pair 9 Facies Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 18 Pedigree Chromosomes, Human, Pair 13 Chromosomes, Fungal Chromosomes, Human, 6-12 and X Chromosomes, Plant Chromosomes, Human, Pair 16 WAGR Syndrome Chromosomes, Human, Pair 2 Hypocalcemia Catechol O-Methyltransferase Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 10 Muscle Hypotonia Chromosomes, Human, Pair 5 Translocation, Genetic Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 8 Chromosomes, Mammalian Chromosomes, Human, X Chromosome Pairing Heart Defects, Congenital Eye Abnormalities Chromosomes, Artificial, Bacterial Chromosomes, Human, Pair 19 Schizophrenia Monosomy Chromosomes, Human, Pair 12 Down Syndrome T-Box Domain Proteins Chromosomes, Human, 1-3 Comparative Genomic Hybridization Genotype Chromosome Painting Amino Acid Sequence Genetic Linkage Chromosomes, Human, Pair 14 Chromosomes, Artificial, Yeast Stanford-Binet Test Exostoses, Multiple Hereditary Chromosomes, Human, Pair 20 Genetic Markers Learning Disorders Gene Dosage Chromosomes, Human, 16-18 Chromosomes, Human, 13-15 Chromosome Inversion Gene Rearrangement Metabolic Syndrome X Language Development Disorders Chromosomes, Human, 21-22 and Y

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