Carriers 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

Diseases27

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 Genomic Instability Anemia, Megaloblastic Chromosome Aberrations Anemia, Refractory Nijmegen Breakage Syndrome Pancytopenia Anemia, Hemolytic, Congenital Oculocerebrorenal Syndrome Equine Infectious Anemia DNA Repair-Deficiency Disorders Genetic Predisposition to Disease

Chemicals and Drugs35

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment4

Hemibody Irradiation Genetic Complementation Test Drug Carriers Heterozygote Detection

Phenomena and Processes20

DNA Repair DNA Damage Chromosome Breakage Ubiquitination Mutation Chromosomal Instability Genomic Instability Heterozygote Homologous Recombination Chromosome Aberrations Genes, BRCA2 DNA Breaks, Double-Stranded Genes, BRCA1 Sister Chromatid Exchange DNA Replication Phenotype Protein Binding Recombination, Genetic Base Sequence Genetic Predisposition to Disease

Information Science2

Molecular Sequence Data Base Sequence

Named Groups2

Health Care1

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

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