Child with deletion 3q syndrome chromosome deletion. Medical search. Frequent questions

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Anatomy53

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

Organisms5

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

Diseases44

Laryngomalacia Chromosome Deletion Trisomy Sex Chromosome Disorders of Sex Development Oligospermia Sex Chromosome Aberrations Syndrome Chromosome Aberrations Infertility, Male Chromosome Disorders Down Syndrome Chromosome Breakage Abnormalities, Multiple Metabolic Syndrome X Chromosome Inversion Ring Chromosomes Translocation, Genetic DiGeorge Syndrome Intellectual Disability Nephrotic Syndrome Turner Syndrome Aneuploidy Prader-Willi Syndrome Sjogren's Syndrome Williams Syndrome Myelodysplastic Syndromes Genetic Predisposition to Disease Angelman Syndrome Chromosome Duplication Chromosome Fragility Klinefelter Syndrome Nondisjunction, Genetic Monosomy Facies Chromosomal Instability Cushing Syndrome Craniofacial Abnormalities Growth Disorders 22q11 Deletion Syndrome Polycystic Ovary Syndrome Acute Coronary Syndrome Child Nutrition Disorders Microcephaly Long QT Syndrome

Chemicals and Drugs26

Genetic Markers DNA DNA-Binding Proteins DNA Primers Transcription Factors Nuclear Proteins Bacterial Proteins RNA, Messenger DNA Probes DNA Transposable Elements DNA, Bacterial Saccharomyces cerevisiae Proteins Chromosomal Proteins, Non-Histone Complement C1q Cell Cycle Proteins DNA, Satellite Carrier Proteins DNA Restriction Enzymes DNA, Neoplasm Recombinant Fusion Proteins Membrane Proteins Fungal Proteins DNA, Complementary DNA, Fungal Proteins Repressor Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment34

Chromosome Mapping Karyotyping In Situ Hybridization, Fluorescence Chromosome Banding Chromosome Painting Pedigree Polymerase Chain Reaction Cloning, Molecular DNA Mutational Analysis Sequence Analysis, DNA Blotting, Southern Crosses, Genetic Nucleic Acid Hybridization Models, Genetic Genetic Complementation Test Sequence Alignment Risk Factors Case-Control Studies Mutagenesis, Insertional Dental Care for Children Comparative Genomic Hybridization Chromosome Walking Facies Cytogenetic Analysis Genetic Testing Prevalence Transfection Treatment Outcome Retrospective Studies Restriction Mapping Reverse Transcriptase Polymerase Chain Reaction Follow-Up Studies Prospective Studies Mutagenesis, Site-Directed

Psychiatry and Psychology7

Child Behavior Intellectual Disability Child Rearing Child Behavior Disorders Child Psychology Parents Child Language

Phenomena and Processes142

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

Disciplines and Occupations1

Anthropology, Education, Sociology and Social Phenomena2

Child Welfare Parents

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny Prevalence

Named Groups6

Disabled Children Child, Institutionalized Infant, Newborn Child of Impaired Parents Parents Child, Orphaned

Health Care12

Child Health Services Risk Factors Case-Control Studies Dental Care for Children Age Factors Genetic Testing Prevalence Treatment Outcome Retrospective Studies Family Health Follow-Up Studies Prospective Studies

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

Laryngomalacia Chromosome Deletion Trisomy Y Chromosome Gene Deletion Chromosome Mapping Sex Chromosome Disorders of Sex Development Oligospermia Sex Chromosome Aberrations Syndrome Chromosomes Chromosomes, Human, Y Chromosome Aberrations Karyotyping Sequence Deletion Sequence Tagged Sites Infertility, Male In Situ Hybridization, Fluorescence Chromosome Banding X Chromosome Phenotype Chromosomes, Human, Pair 1 Molecular Sequence Data Sex Chromosomes Base Sequence Chromosomes, Human, Pair 7 Chromosomes, Human Chromosomes, Human, Pair 17 Chromosomes, Bacterial Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 9 Chromosome Segregation Mutation Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 21 Chromosome Disorders Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 13 Chromosomes, Fungal Chromosomes, Human, 6-12 and X Chromosomes, Human, Pair 4 Chromosomes, Plant Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 8 Chromosomes, Mammalian Chromosomes, Human, X Down Syndrome Chromosome Pairing Chromosomes, Human, Pair 12 Chromosomes, Artificial, Bacterial Genetic Linkage Chromosomes, Human, Pair 14 Chromosomes, Human, 1-3 Amino Acid Sequence Chromosome Painting Chromosome Breakage Abnormalities, Multiple Chromosomes, Artificial, Yeast Pedigree Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 18 Child Welfare Genetic Markers Chromosomes, Human, 16-18 Chromosomes, Human, 13-15 Metabolic Syndrome X Chromosome Inversion Chromosomes, Human, 21-22 and Y Disabled Children Recombination, Genetic Ring Chromosomes Polymerase Chain Reaction Child Behavior Cloning, Molecular Alleles Chromosomes, Human, 4-5 Translocation, Genetic Genotype DNA Mutational Analysis DiGeorge Syndrome Chromosome Positioning Intellectual Disability DNA Sequence Analysis, DNA X Chromosome Inactivation Microsatellite Repeats Centromere Exons Plasmids Blotting, Southern Nephrotic Syndrome Heterozygote Hybrid Cells Meiosis Homozygote

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