Deletion and allele. Medical search. Frequent questions

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Anatomy26

Cell Line Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 9 Cells, Cultured Chromosomes, Human, Pair 17 X Chromosome Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 3 Chromosomes, Human, Y Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 4 Tumor Cells, Cultured Chromosomes, Bacterial COS Cells Cell Nucleus Chromosomes, Human, Pair 10 Embryo, Mammalian Y Chromosome Chromosomes, Human, Pair 16 Fibroblasts HeLa Cells

Organisms8

Mice, Knockout Saccharomyces cerevisiae Escherichia coli Mice, Inbred C57BL Mice, Mutant Strains Drosophila melanogaster Zea mays Drosophila

Diseases15

Chromosome Deletion Genetic Predisposition to Disease Abnormalities, Multiple 22q11 Deletion Syndrome Syndrome DiGeorge Syndrome Intellectual Disability Chromosome Aberrations Chromosome Disorders Chromosome Breakage Disease Models, Animal Translocation, Genetic Chromosome Inversion Jacobsen Distal 11q Deletion Syndrome Craniofacial Abnormalities

Chemicals and Drugs53

DNA Primers Genetic Markers DNA DNA-Binding Proteins Transcription Factors Bacterial Proteins RNA, Messenger Saccharomyces cerevisiae Proteins Fungal Proteins DNA Transposable Elements HLA-DRB1 Chains Membrane Proteins Nuclear Proteins Recombinant Fusion Proteins Carrier Proteins Repressor Proteins HLA-DR Antigens DNA, Bacterial HLA-DQ Antigens Recombinant Proteins DNA, Fungal Integrases DNA Restriction Enzymes Proteins DNA, Mitochondrial DNA, Complementary Codon HLA-B Antigens Escherichia coli Proteins DNA, Neoplasm Apolipoprotein E4 Trans-Activators Viral Proteins Nerve Tissue Proteins DNA Probes Codon, Nonsense Peptidyl-Dipeptidase A DNA, Viral Drosophila Proteins Deoxyribonucleases, Type II Site-Specific Homeodomain Proteins Membrane Transport Proteins Oligonucleotide Probes Cell Cycle Proteins RNA-Binding Proteins Oligodeoxyribonucleotides Apolipoproteins E DNA, Plant HLA Antigens HLA-DQ alpha-Chains Protein-Serine-Threonine Kinases Green Fluorescent Proteins Tumor Suppressor Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Polymerase Chain Reaction Chromosome Mapping DNA Mutational Analysis Sequence Analysis, DNA Cloning, Molecular Pedigree Models, Genetic Genetic Complementation Test Crosses, Genetic Restriction Mapping Blotting, Southern Case-Control Studies Mutagenesis, Insertional In Situ Hybridization, Fluorescence Sequence Alignment Mutagenesis, Site-Directed Genetic Association Studies Heterozygote Detection Transfection Genetic Testing Gene Targeting Nucleic Acid Hybridization Karyotyping Reverse Transcriptase Polymerase Chain Reaction Risk Factors Genome-Wide Association Study Comparative Genomic Hybridization Blotting, Western Chromosome Banding Disease Models, Animal Physical Chromosome Mapping Gene Knockout Techniques Cohort Studies Oligonucleotide Array Sequence Analysis Models, Biological Pigmentation Blotting, Northern

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes138

Alleles Gene Deletion Sequence Deletion Chromosome Deletion Mutation Base Sequence Genotype Polymorphism, Genetic Gene Frequency Phenotype Amino Acid Sequence Homozygote Polymorphism, Single Nucleotide Heterozygote Genetic Predisposition to Disease Genetic Variation Haplotypes Exons Promoter Regions, Genetic Genetic Markers Recombination, Genetic Microsatellite Repeats Plasmids Mutagenesis Transcription, Genetic Polymorphism, Restriction Fragment Length Point Mutation Linkage Disequilibrium Clonal Deletion Frameshift Mutation Mutagenesis, Insertional Chromosomes, Human, Pair 22 Genes, Lethal Genetic Linkage Sequence Homology, Amino Acid Genes Genes, Fungal Genes, Bacterial Repetitive Sequences, Nucleic Acid Gene Dosage Introns DNA Transposable Elements Gene Expression Regulation Genetic Loci Protein Structure, Tertiary Genes, Dominant Suppression, Genetic Transfection Binding Sites Protein Binding Genes, Recessive INDEL Mutation Mutation, Missense Sequence Homology, Nucleic Acid Loss of Heterozygosity Selection, Genetic Gene Expression Chromosomes, Human, Pair 9 Polymorphism, Single-Stranded Conformational Multigene Family Phylogeny Signal Transduction Gene Expression Regulation, Bacterial Evolution, Molecular Gene Expression Regulation, Fungal Gene Rearrangement Nucleic Acid Hybridization Chromosome Aberrations Species Specificity Genes, Regulator Chromosomes, Human, Pair 17 X Chromosome Minisatellite Repeats Chromosomes, Human, Pair 11 Gene Expression Regulation, Developmental Codon Virulence Genes, Plant Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 1 Operon Chromosomes, Human, Pair 3 Genes, Viral Open Reading Frames Regulatory Sequences, Nucleic Acid Conserved Sequence Genome, Human Genes, Suppressor Chromosome Breakage Structure-Activity Relationship Chromosomes, Human, Y Gene Duplication Genes, Tumor Suppressor Epistasis, Genetic Mosaicism Genes, Reporter RNA Splicing DNA Copy Number Variations Quantitative Trait Loci Tandem Repeat Sequences Chromosomes, Human, Pair 5 Codon, Nonsense Chromosomes, Human, Pair 6 Transformation, Genetic Chromosomes, Human, Pair 7 Haploidy Chromosomes, Human, Pair 15 DNA Replication Haploinsufficiency Translocation, Genetic Dinucleotide Repeats Virus Replication Chromosomes, Human, Pair 4 Germ-Line Mutation Temperature DNA Repair Diploidy Genetic Vectors Inheritance Patterns Time Factors Chromosomes, Bacterial Penetrance Founder Effect Chromosomes, Human, Pair 10 Biological Evolution Enhancer Elements, Genetic Y Chromosome Chromosome Inversion Chromosomes, Human, Pair 16 Pseudogenes Genes, Insect Alternative Splicing Trinucleotide Repeats Pigmentation Nucleic Acid Conformation Transcriptional Activation Kinetics DNA Methylation

Disciplines and Occupations1

Genetics, Population

Technology, Industry, Agriculture1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny

Named Groups3

Asian Continental Ancestry Group European Continental Ancestry Group African Continental Ancestry Group

Health Care7

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

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Alleles Gene Deletion Sequence Deletion Chromosome Deletion Molecular Sequence Data Mutation Base Sequence Genotype Polymorphism, Genetic Gene Frequency Phenotype Amino Acid Sequence Polymerase Chain Reaction Chromosome Mapping Homozygote Polymorphism, Single Nucleotide Heterozygote Genetic Predisposition to Disease Genetic Variation Haplotypes DNA Mutational Analysis Exons DNA Primers Sequence Analysis, DNA Promoter Regions, Genetic Cloning, Molecular Pedigree Genetic Markers Models, Genetic Recombination, Genetic Microsatellite Repeats Plasmids Genetic Complementation Test Mice, Knockout Saccharomyces cerevisiae Mutagenesis Transcription, Genetic DNA Crosses, Genetic Polymorphism, Restriction Fragment Length Point Mutation Escherichia coli Restriction Mapping DNA-Binding Proteins Cell Line Transcription Factors Blotting, Southern Case-Control Studies Linkage Disequilibrium Clonal Deletion Bacterial Proteins RNA, Messenger Frameshift Mutation Mutagenesis, Insertional Chromosomes, Human, Pair 22 Genes, Lethal Mice, Inbred C57BL Genetic Linkage Saccharomyces cerevisiae Proteins Sequence Homology, Amino Acid Genes Genes, Fungal Genes, Bacterial Repetitive Sequences, Nucleic Acid Gene Dosage In Situ Hybridization, Fluorescence Introns Fungal Proteins Sequence Alignment DNA Transposable Elements HLA-DRB1 Chains Gene Expression Regulation Abnormalities, Multiple Genetic Loci Protein Structure, Tertiary Mutagenesis, Site-Directed Genetic Association Studies Genetics, Population Membrane Proteins Heterozygote Detection Genes, Dominant Suppression, Genetic Transfection Binding Sites Protein Binding Genes, Recessive 22q11 Deletion Syndrome Asian Continental Ancestry Group Nuclear Proteins Syndrome Recombinant Fusion Proteins Carrier Proteins INDEL Mutation Mutation, Missense Sequence Homology, Nucleic Acid DiGeorge Syndrome Loss of Heterozygosity Selection, Genetic Gene Expression Genetic Testing

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