Recessive fanconi anemia. Medical search. Frequent questions

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Anatomy6

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

Organisms1

Infectious Anemia Virus, Equine

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, Sickle Cell Anemia, Diamond-Blackfan Anemia, Sideroblastic Chromosomal Instability Anemia, Megaloblastic Genomic Instability Chromosome Aberrations Nijmegen Breakage Syndrome Anemia, Refractory Pancytopenia Syndrome Anemia, Hemolytic, Congenital Oculocerebrorenal Syndrome DNA Repair-Deficiency Disorders Cystinosis Equine Infectious Anemia Anemia, Dyserythropoietic, Congenital

Chemicals and Drugs32

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 Ubiquitin-Specific Proteases Epoxy Compounds BRCA2 Protein Proteins Ubiquitin Rad51 Recombinase DNA Helicases BRCA1 Protein Recombinases Hemoglobins Basic-Leucine Zipper Transcription Factors Trioxsalen Nucleic Acid Synthesis Inhibitors Methoxsalen Ataxia Telangiectasia Mutated Proteins DNA Alkylating Agents Erythropoietin Ficusin

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Hemibody Irradiation Genetic Complementation Test Pedigree DNA Mutational Analysis Chromosome Mapping

Phenomena and Processes24

Genes, Recessive DNA Repair DNA Damage Mutation Chromosome Breakage Consanguinity Ubiquitination Phenotype Chromosomal Instability Homozygote Genomic Instability Homologous Recombination Chromosome Aberrations Heterozygote Base Sequence DNA Breaks, Double-Stranded Alleles Sister Chromatid Exchange DNA Replication Recombination, Genetic Genetic Heterogeneity Protein Binding Mutation, Missense Exons

Information Science2

Molecular Sequence Data Base Sequence

Named Groups2

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

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 Genes, Recessive Fanconi Anemia Complementation Group F Protein Fanconi Anemia Complementation Group E Protein Mitomycin Anemia, Aplastic DNA Repair Anemia, Hemolytic DNA Damage Cross-Linking Reagents Hemibody Irradiation Nuclear Proteins Mutation DNA-Binding Proteins Cell Cycle Proteins Anemia, Hemolytic, Autoimmune Bone Marrow Diseases Anemia, Hypochromic Chromosome Breakage Consanguinity Ubiquitin-Specific Proteases Anemia, Macrocytic Epoxy Compounds BRCA2 Protein Anemia, Pernicious Ubiquitination Genetic Complementation Test Pedigree Bloom Syndrome Proteins Ubiquitin Anemia, Sickle Cell Anemia, Diamond-Blackfan Anemia, Sideroblastic Phenotype Rad51 Recombinase Chromosomal Instability Homozygote Anemia, Megaloblastic Genomic Instability DNA Helicases Gypsies BRCA1 Protein Homologous Recombination Recombinases Cell Line Molecular Sequence Data Chromosome Aberrations Infectious Anemia Virus, Equine Hemoglobins Nijmegen Breakage Syndrome Hematopoietic Stem Cells Anemia, Refractory DNA Mutational Analysis HeLa Cells Basic-Leucine Zipper Transcription Factors Heterozygote Pancytopenia Jews Cell Line, Transformed Fibroblasts Base Sequence Trioxsalen Syndrome Nucleic Acid Synthesis Inhibitors DNA Breaks, Double-Stranded Alleles Sister Chromatid Exchange DNA Replication Methoxsalen Anemia, Hemolytic, Congenital Recombination, Genetic Ataxia Telangiectasia Mutated Proteins DNA Lymphocytes Oculocerebrorenal Syndrome Genetic Heterogeneity DNA Repair-Deficiency Disorders Cystinosis Protein Binding Equine Infectious Anemia Alkylating Agents Anemia, Dyserythropoietic, Congenital Erythropoietin Ficusin Chromosome Mapping Mutation, Missense Exons

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