Mutations fanconi anemia. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy8

Cell Line HeLa Cells Hematopoietic Stem Cells Cell Line, Transformed Fibroblasts Lymphocytes Cell Nucleus Cells, Cultured

Organisms3

Infectious Anemia Virus, Equine Mice, Knockout Chicken anemia virus

Diseases29

Fanconi Anemia Fanconi Syndrome Anemia Anemia, Aplastic Anemia, Hemolytic Anemia, Hemolytic, Autoimmune Bone Marrow Diseases Anemia, Hypochromic Chromosome Breakage Anemia, Macrocytic Anemia, Pernicious Bloom Syndrome Anemia, Diamond-Blackfan Anemia, Sickle Cell Anemia, Sideroblastic Genomic Instability Chromosomal Instability Anemia, Megaloblastic Chromosome Aberrations Anemia, Refractory Nijmegen Breakage Syndrome Pancytopenia Genetic Predisposition to Disease Syndrome Anemia, Hemolytic, Congenital Oculocerebrorenal Syndrome DNA Repair-Deficiency Disorders Equine Infectious Anemia Anemia, Dyserythropoietic, Congenital

Chemicals and Drugs36

Fanconi Anemia Complementation Group Proteins Fanconi Anemia Complementation Group C Protein Fanconi Anemia Complementation Group D2 Protein Fanconi Anemia Complementation Group A Protein Fanconi Anemia Complementation Group G Protein Fanconi Anemia Complementation Group L Protein Fanconi Anemia Complementation Group F Protein Fanconi Anemia Complementation Group E Protein Mitomycin Cross-Linking Reagents Nuclear Proteins DNA-Binding Proteins Cell Cycle Proteins BRCA2 Protein Proteins Ubiquitin-Specific Proteases Epoxy Compounds Ubiquitin BRCA1 Protein Rad51 Recombinase DNA Helicases Recombinases DNA Hemoglobins Basic-Leucine Zipper Transcription Factors Trioxsalen Nucleic Acid Synthesis Inhibitors Methoxsalen DNA Primers Ataxia Telangiectasia Mutated Proteins Alkylating Agents Recombinant Proteins Erythropoietin Ficusin Codon, Nonsense Mutagens

Analytical, Diagnostic and Therapeutic Techniques and Equipment11

Hemibody Irradiation Genetic Complementation Test Pedigree DNA Mutational Analysis Amino Acid Substitution Polymerase Chain Reaction Genetic Testing Transfection Mutagenesis, Site-Directed Sequence Analysis, DNA Chromosome Mapping

Phenomena and Processes47

Point Mutation Mutation, Missense Mutation DNA Repair DNA Damage Germ-Line Mutation Frameshift Mutation Chromosome Breakage Ubiquitination Base Sequence Heterozygote Exons Alleles Genomic Instability Chromosomal Instability Genes, Recessive Phenotype Amino Acid Substitution Amino Acid Sequence Protein Binding Homozygote Homologous Recombination Mutation Rate Chromosome Aberrations Genotype Recombination, Genetic Sequence Deletion Mutagenesis DNA Replication Genes, BRCA2 Protein Structure, Tertiary Genes, BRCA1 Signal Transduction DNA Breaks, Double-Stranded Genetic Predisposition to Disease Sister Chromatid Exchange Transfection Founder Effect Gene Deletion Polymorphism, Single-Stranded Conformational Consanguinity Genetic Heterogeneity Mosaicism Drug Resistance Cell Cycle Codon, Nonsense Sequence Homology, Amino Acid

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups2

Health Care1

Genetic Testing

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

Fanconi Anemia Fanconi Anemia Complementation Group Proteins Fanconi Anemia Complementation Group C Protein Fanconi Anemia Complementation Group D2 Protein Fanconi Anemia Complementation Group A Protein Fanconi Anemia Complementation Group G Protein Fanconi Syndrome Fanconi Anemia Complementation Group L Protein Anemia Fanconi Anemia Complementation Group F Protein Fanconi Anemia Complementation Group E Protein Mitomycin Point Mutation Mutation, Missense Anemia, Aplastic Mutation DNA Repair Anemia, Hemolytic Cross-Linking Reagents Nuclear Proteins DNA-Binding Proteins DNA Damage Hemibody Irradiation Germ-Line Mutation Frameshift Mutation Cell Cycle Proteins BRCA2 Protein Anemia, Hemolytic, Autoimmune Genetic Complementation Test Pedigree Bone Marrow Diseases Anemia, Hypochromic Chromosome Breakage Proteins Ubiquitin-Specific Proteases Ubiquitination Anemia, Macrocytic Epoxy Compounds Anemia, Pernicious Base Sequence Molecular Sequence Data Cell Line Heterozygote Bloom Syndrome Exons DNA Mutational Analysis Ubiquitin Anemia, Diamond-Blackfan BRCA1 Protein Anemia, Sickle Cell Anemia, Sideroblastic Alleles Genomic Instability Chromosomal Instability Rad51 Recombinase Genes, Recessive DNA Helicases Phenotype Amino Acid Substitution Polymerase Chain Reaction Amino Acid Sequence Protein Binding HeLa Cells Homozygote Recombinases Anemia, Megaloblastic Gypsies Homologous Recombination DNA Jews Mutation Rate Chromosome Aberrations Genotype Hemoglobins Infectious Anemia Virus, Equine Recombination, Genetic Hematopoietic Stem Cells Anemia, Refractory Sequence Deletion Mutagenesis Basic-Leucine Zipper Transcription Factors DNA Replication Cell Line, Transformed Fibroblasts Nijmegen Breakage Syndrome Genes, BRCA2 Pancytopenia Protein Structure, Tertiary Genes, BRCA1 Signal Transduction DNA Breaks, Double-Stranded Trioxsalen Genetic Predisposition to Disease Nucleic Acid Synthesis Inhibitors Genetic Testing Methoxsalen Sister Chromatid Exchange DNA Primers Transfection Syndrome

No FAQ available that match "mutations fanconi anemia"