Syndrome and ataxia telangiectasia are autosomal recessive. Medical search. Frequent questions

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Anatomy22

Fibroblasts Cell Line Cells, Cultured Cell Line, Transformed Chromosomes, Human, Pair 11 Cell Line, Tumor Lymphocytes Cerebellum HeLa Cells Telomere Chromosomes, Human, Pair 14 Cell Nucleus Chromosomes, Human, Pair 2 Chromatin Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 9 Skin HCT116 Cells Fundus Oculi Brain Chromosomes, Human, Pair 19 HEK293 Cells

Organisms5

Mice, Knockout Mice, Mutant Strains Mice, 129 Strain Mice, Inbred C57BL Mice, Transgenic

Diseases79

Ataxia Telangiectasia Telangiectasis Telangiectasia, Hereditary Hemorrhagic Ataxia Syndrome Cerebellar Ataxia Retinal Telangiectasis Friedreich Ataxia Spinocerebellar Ataxias Gait Ataxia Microcephaly Polycystic Kidney, Autosomal Recessive Epistaxis Abnormalities, Multiple Arteriovenous Malformations Nijmegen Breakage Syndrome CREST Syndrome Chromosome Aberrations Retinitis Pigmentosa Chromosome Disorders Chromosome Breakage Down Syndrome Metabolic Syndrome X Immunologic Deficiency Syndromes Intellectual Disability Ichthyosis Hypotrichosis Genomic Instability Nephrotic Syndrome Ichthyosiform Erythroderma, Congenital Deafness Dwarfism Retinal Diseases Hearing Loss, Sensorineural Cardiac Output, High Sjogren's Syndrome Ichthyosis, Lamellar Osteochondrodysplasias Disease Models, Animal Bone Diseases, Developmental Muscular Dystrophies Eye Abnormalities Werner Syndrome Nails, Malformed Facies Ectodermal Dysplasia Genetic Predisposition to Disease Turner Syndrome Bloom Syndrome Eye Diseases, Hereditary Metabolism, Inborn Errors Optic Atrophy Osteopetrosis Craniofacial Abnormalities Muscle Hypotonia Hand Deformities, Congenital Bardet-Biedl Syndrome Syndactyly Machado-Joseph Disease Usher Syndromes Translocation, Genetic Charcot-Marie-Tooth Disease Foot Deformities, Congenital Spastic Paraplegia, Hereditary Lymphoma Albinism, Oculocutaneous Chromosomal Instability Myelodysplastic Syndromes Angiodysplasia Kidney Diseases, Cystic Retinal Degeneration Genetic Diseases, Inborn Cushing Syndrome Hearing Loss Microphthalmos Cutis Laxa Dysostoses Cystinosis Amino Acid Metabolism, Inborn Errors

Chemicals and Drugs53

Ataxia Telangiectasia Mutated Proteins Tumor Suppressor Proteins Cell Cycle Proteins Protein-Serine-Threonine Kinases DNA-Binding Proteins Checkpoint Kinase 2 Tumor Suppressor Protein p53 DNA-Activated Protein Kinase Pyrones Activin Receptors, Type II Nuclear Proteins Histones Streptonigrin Protein Kinases DNA Proteins Iron-Binding Proteins DNA Repair Enzymes Codon, Nonsense Nucleic Acid Synthesis Inhibitors Replication Protein A Intracellular Signaling Peptides and Proteins Telomeric Repeat Binding Protein 2 Aphidicolin Hydroxyurea Activin Receptors, Type I Morpholines Alkylating Agents Serine Bleomycin Caffeine DNA Primers Genetic Markers RNA, Small Interfering Carrier Proteins DNA Ligases Chromosomal Proteins, Non-Histone RNA, Messenger Nerve Tissue Proteins Chromatin BRCA1 Protein Cyclin-Dependent Kinase Inhibitor p21 Receptors, Cell Surface Camptothecin Poly(ADP-ribose) Polymerases cdc25 Phosphatases Phosphatidylinositol 3-Kinases Eye Proteins Sarcoglycans Topoisomerase I Inhibitors Membrane Proteins Threonine Enzyme Inhibitors

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

Pedigree DNA Mutational Analysis Chromosome Mapping Dose-Response Relationship, Radiation Heterozygote Detection Genetic Testing Comet Assay Blotting, Western Karyotyping Disease Models, Animal Polymerase Chain Reaction Models, Biological Immunoblotting Facies Magnetic Resonance Imaging Transfection In Situ Hybridization, Fluorescence Sequence Analysis, DNA Flow Cytometry Electroretinography Cloning, Molecular Fluorescein Angiography Fatal Outcome Reverse Transcriptase Polymerase Chain Reaction

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes82

Genes, Recessive DNA Damage Consanguinity Mutation Radiation, Ionizing Homozygote DNA Repair Gamma Rays Radiation Tolerance Phenotype Heterozygote Mutation, Missense DNA Breaks, Double-Stranded Phosphorylation Genetic Linkage Cell Cycle Dose-Response Relationship, Radiation Base Sequence Chromosome Aberrations Exons Signal Transduction Chromosome Breakage Lod Score Alleles DNA Replication Genotype G2 Phase Ultraviolet Rays Apoptosis Genes, Dominant Amino Acid Sequence Chromosomes, Human, Pair 11 X-Rays Haplotypes Infrared Rays Codon, Nonsense Cell Survival Genes, cdc Genomic Instability S Phase Frameshift Mutation Telomere G2 Phase Cell Cycle Checkpoints Gene Deletion Sequence Deletion Cell Cycle Checkpoints Chromosomes, Human, Pair 14 Founder Effect Genetic Heterogeneity Recombination, Genetic Genetic Markers Exome Microsatellite Repeats Oxidative Stress Point Mutation RNA Interference Cell Aging Protein Binding Chromosomes, Human, Pair 2 Time Factors Enzyme Activation Polymorphism, Single-Stranded Conformational Genetic Predisposition to Disease G1 Phase Chromatin Chromosomes, Human, Pair 1 Mitosis Translocation, Genetic Transfection Chromosomes, Human, Pair 9 Trinucleotide Repeat Expansion Chromosomal Instability Protein Structure, Tertiary Gene Rearrangement, T-Lymphocyte Leucine Zippers Trinucleotide Repeats Cell Division Gene Expression Chromosomes, Human, Pair 19 Gene Expression Regulation Introns Down-Regulation

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Fatal Outcome

Named Groups2

Infant, Newborn Arabs

Health Care7

Dose-Response Relationship, Radiation Ultraviolet Rays Infrared Rays Genetic Testing Age of Onset Family Health Fatal Outcome

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

Ataxia Telangiectasia Ataxia Telangiectasia Mutated Proteins Telangiectasis Telangiectasia, Hereditary Hemorrhagic Genes, Recessive Ataxia Syndrome Cerebellar Ataxia Tumor Suppressor Proteins Cell Cycle Proteins Protein-Serine-Threonine Kinases Retinal Telangiectasis Friedreich Ataxia DNA-Binding Proteins DNA Damage Consanguinity Pedigree Spinocerebellar Ataxias Mutation Radiation, Ionizing Gait Ataxia Checkpoint Kinase 2 Homozygote DNA Repair Microcephaly Gamma Rays Radiation Tolerance Phenotype Heterozygote DNA Mutational Analysis Polycystic Kidney, Autosomal Recessive Mutation, Missense Tumor Suppressor Protein p53 DNA Breaks, Double-Stranded Phosphorylation DNA-Activated Protein Kinase Epistaxis Abnormalities, Multiple Fibroblasts Pyrones Arteriovenous Malformations Activin Receptors, Type II Nuclear Proteins Nijmegen Breakage Syndrome Histones Molecular Sequence Data Genetic Linkage Cell Line Cell Cycle Chromosome Mapping Dose-Response Relationship, Radiation Base Sequence CREST Syndrome Chromosome Aberrations Streptonigrin Retinitis Pigmentosa Chromosome Disorders Exons Signal Transduction Protein Kinases Chromosome Breakage Lod Score Alleles DNA Replication Down Syndrome Metabolic Syndrome X Cells, Cultured Genotype G2 Phase Immunologic Deficiency Syndromes Ultraviolet Rays DNA Apoptosis Intellectual Disability Genes, Dominant Amino Acid Sequence Proteins Cell Line, Transformed Chromosomes, Human, Pair 11 X-Rays Mice, Knockout Ichthyosis Iron-Binding Proteins Cell Line, Tumor DNA Repair Enzymes Haplotypes Lymphocytes Infrared Rays Codon, Nonsense Nucleic Acid Synthesis Inhibitors Cell Survival Genes, cdc Replication Protein A Hypotrichosis Genomic Instability S Phase Cerebellum Frameshift Mutation Heterozygote Detection Nephrotic Syndrome

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