22q11 microdeletion. Medical search. Frequent questions

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Anatomy24

Chromosomes, Human, Pair 22 Chromosomes, Human, Y Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 2 Y Chromosome Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 14 Chromosomes, Artificial, Bacterial Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 9 Face X Chromosome Testis Spermatozoa Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 18

Diseases49

Chromosome Deletion DiGeorge Syndrome Abnormalities, Multiple Intellectual Disability Sex Chromosome Disorders of Sex Development Syndrome Williams Syndrome Facies Azoospermia Oligospermia Sex Chromosome Aberrations Osteopoikilosis Chromosome Duplication Craniofacial Abnormalities Truncus Arteriosus, Persistent Chromosome Disorders Muscle Hypotonia Pulmonary Atresia Infertility, Male Heart Defects, Congenital Chromosome Breakage Chromosome Aberrations Pseudohypoparathyroidism 46, XX Disorders of Sex Development Abnormal Karyotype Neurofibromatosis 1 Tetralogy of Fallot Fibrous Dysplasia, Polyostotic Prader-Willi Syndrome Foot Deformities, Congenital Brachydactyly Smith-Magenis Syndrome Hand Deformities, Congenital Aortic Stenosis, Supravalvular Heart Septal Defects, Ventricular Angelman Syndrome Cleft Palate Rubinstein-Taybi Syndrome Androgen-Insensitivity Syndrome Dwarfism Hypocalcemia Growth Disorders Congenital Abnormalities Chromosome Inversion Genetic Predisposition to Disease Fetal Diseases Seizures Translocation, Genetic Heart Septal Defects, Atrial

Chemicals and Drugs14

Seminal Plasma Proteins Neurofibromin 1 Complement C1q Cerebroside-Sulfatase Genetic Markers Molecular Probes DNA Nerve Tissue Proteins Nuclear Proteins Transcription Factors DNA-Binding Proteins Membrane Proteins Ubiquinone GTP-Binding Protein alpha Subunits, Gq-G11

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Facies Comparative Genomic Hybridization In Situ Hybridization, Fluorescence Pedigree Karyotyping Primed In Situ Labeling Chromosome Mapping Chromosome Banding Polymerase Chain Reaction Physical Chromosome Mapping Genetic Testing Sperm Injections, Intracytoplasmic DNA Mutational Analysis Oligonucleotide Array Sequence Analysis Genetic Association Studies Prenatal Diagnosis Nucleic Acid Hybridization Sequence Analysis, DNA Case-Control Studies Reverse Transcriptase Polymerase Chain Reaction Magnetic Resonance Imaging Prevalence

Psychiatry and Psychology5

Intellectual Disability Developmental Disabilities 46, XX Disorders of Sex Development Autistic Disorder Schizophrenia

Phenomena and Processes68

Chromosome Deletion Chromosomes, Human, Pair 22 Chromosomes, Human, Y Chromosomes, Human, Pair 15 Sex Chromosome Aberrations Gene Deletion Chromosome Duplication Chromosomes, Human, Pair 16 Sequence Tagged Sites Sequence Deletion Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 2 Chromosome Breakage Chromosome Aberrations Chromosome Breakpoints Phenotype Y Chromosome Segmental Duplications, Genomic Abnormal Karyotype Chromosomes, Human, Pair 7 Haploinsufficiency Gene Duplication Genetic Loci Mosaicism Genes, Neurofibromatosis 1 Cosmids Haplotypes Chromosomes, Human, Pair 14 Chromosomes, Artificial, Bacterial DNA Copy Number Variations Chromosomes, Human, Pair 20 Gene Dosage Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 3 Genomic Imprinting Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 5 Homologous Recombination Spermatogenesis Microsatellite Repeats Base Sequence Exons Chromosome Inversion Gene Rearrangement Chromosomes, Human, Pair 9 Mutation Genetic Predisposition to Disease Pregnancy Genetic Markers Genotype Polymorphism, Single Nucleotide X Chromosome Alleles Genome, Human Heterozygote Translocation, Genetic Polymorphism, Genetic Gene Frequency Homozygote Nucleic Acid Hybridization Recombination, Genetic Amino Acid Sequence Chromosomes, Human, Pair 4 Genetic Linkage Chromosomes, Human, Pair 10 Lod Score Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 18

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care3

Genetic Testing Case-Control Studies Prevalence

Geographicals1

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

Chromosome Deletion Chromosomes, Human, Pair 22 DiGeorge Syndrome Abnormalities, Multiple Intellectual Disability Sex Chromosome Disorders of Sex Development Chromosomes, Human, Y Syndrome Williams Syndrome Facies Comparative Genomic Hybridization In Situ Hybridization, Fluorescence Azoospermia Chromosomes, Human, Pair 15 Oligospermia Sex Chromosome Aberrations Gene Deletion Seminal Plasma Proteins Osteopoikilosis Chromosome Duplication Craniofacial Abnormalities Chromosomes, Human, Pair 16 Truncus Arteriosus, Persistent Chromosome Disorders Developmental Disabilities Pedigree Muscle Hypotonia Pulmonary Atresia Sequence Tagged Sites Sequence Deletion Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 2 Infertility, Male Heart Defects, Congenital Karyotyping Chromosome Breakage Chromosome Aberrations Chromosome Breakpoints Phenotype Y Chromosome Segmental Duplications, Genomic Pseudohypoparathyroidism 46, XX Disorders of Sex Development Abnormal Karyotype Chromosomes, Human, Pair 7 Neurofibromatosis 1 Tetralogy of Fallot Fibrous Dysplasia, Polyostotic Prader-Willi Syndrome Haploinsufficiency Neurofibromin 1 Primed In Situ Labeling Gene Duplication Genetic Loci Complement C1q Chromosome Mapping Chromosome Banding Mosaicism Foot Deformities, Congenital Brachydactyly Smith-Magenis Syndrome Hand Deformities, Congenital Polymerase Chain Reaction Autistic Disorder Aortic Stenosis, Supravalvular Genes, Neurofibromatosis 1 Heart Septal Defects, Ventricular Angelman Syndrome Physical Chromosome Mapping Cosmids Cleft Palate Haplotypes Genetic Testing Chromosomes, Human, Pair 14 Chromosomes, Artificial, Bacterial Infant, Newborn DNA Copy Number Variations Chromosomes, Human, Pair 20 Cerebroside-Sulfatase Rubinstein-Taybi Syndrome Gene Dosage Sperm Injections, Intracytoplasmic Androgen-Insensitivity Syndrome Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 3 DNA Mutational Analysis Genomic Imprinting Chromosomes, Human, Pair 1 Dwarfism Chromosomes, Human, Pair 5 Oligonucleotide Array Sequence Analysis Hypocalcemia Molecular Sequence Data Homologous Recombination Spermatogenesis Microsatellite Repeats Growth Disorders Congenital Abnormalities Base Sequence Genetic Association Studies

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