Genetic syndrome fanconi anemia. Medical search. Frequent questions

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Anatomy8

Chromosomes, Human, Pair 22 Cell Line Hematopoietic Stem Cells HeLa Cells Cell Line, Transformed Fibroblasts Lymphocytes Bone Marrow

Organisms2

Infectious Anemia Virus, Equine Chicken anemia virus

Diseases40

Fanconi Anemia Syndrome Costello Syndrome Fanconi Syndrome Anemia Prurigo Abnormalities, Multiple Anemia, Aplastic Genetic Diseases, Inborn Chromosome Aberrations Chromosome Disorders Fetal Diseases Heart Defects, Congenital Anemia, Hemolytic Anemia, Hemolytic, Autoimmune Bone Marrow Diseases Bloom Syndrome Chromosome Breakage Anemia, Hypochromic Anemia, Macrocytic Anemia, Pernicious Down Syndrome Metabolic Syndrome X Anemia, Sickle Cell Anemia, Diamond-Blackfan Anemia, Sideroblastic Chromosomal Instability Genomic Instability Myelodysplastic Syndromes Anemia, Megaloblastic Nijmegen Breakage Syndrome Pancytopenia Oculocerebrorenal Syndrome Anemia, Refractory Nephrotic Syndrome Sjogren's Syndrome Anemia, Hemolytic, Congenital DNA Repair-Deficiency Disorders Equine Infectious Anemia Turner Syndrome

Chemicals and Drugs33

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 BRCA2 Protein Epoxy Compounds 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 Erythropoietin Alkylating Agents RecQ Helicases Ficusin

Analytical, Diagnostic and Therapeutic Techniques and Equipment4

Pedigree Hemibody Irradiation Genetic Complementation Test DNA Mutational Analysis

Psychiatry and Psychology1

Developmental Disabilities

Phenomena and Processes21

Chromosomes, Human, Pair 22 Chromosome Aberrations Mutation DNA Repair DNA Damage Pregnancy Chromosome Breakage Ubiquitination Chromosomal Instability Genomic Instability Homologous Recombination Phenotype DNA Breaks, Double-Stranded Sister Chromatid Exchange DNA Replication Protein Binding Genes, Recessive Recombination, Genetic Base Sequence Mosaicism Genes, BRCA2

Information Science2

Molecular Sequence Data Base Sequence

Named Groups3

Infant, Newborn Gypsies Jews

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology 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 Syndrome Fanconi Anemia Complementation Group G Protein Costello Syndrome Fanconi Syndrome Fanconi Anemia Complementation Group L Protein Anemia Fanconi Anemia Complementation Group F Protein Fanconi Anemia Complementation Group E Protein Prurigo Mitomycin Abnormalities, Multiple Chromosomes, Human, Pair 22 Anemia, Aplastic Genetic Diseases, Inborn Chromosome Aberrations Developmental Disabilities Chromosome Disorders Fetal Diseases Pedigree Heart Defects, Congenital Mutation DNA Repair Anemia, Hemolytic Infant, Newborn DNA Damage Cross-Linking Reagents Hemibody Irradiation Nuclear Proteins DNA-Binding Proteins Pregnancy Anemia, Hemolytic, Autoimmune Bone Marrow Diseases Cell Cycle Proteins Bloom Syndrome Chromosome Breakage Anemia, Hypochromic Anemia, Macrocytic Ubiquitin-Specific Proteases BRCA2 Protein Anemia, Pernicious Epoxy Compounds Ubiquitination Down Syndrome Metabolic Syndrome X Proteins Anemia, Sickle Cell Genetic Complementation Test Anemia, Diamond-Blackfan Ubiquitin Anemia, Sideroblastic Chromosomal Instability Rad51 Recombinase DNA Helicases Genomic Instability Myelodysplastic Syndromes BRCA1 Protein Homologous Recombination Anemia, Megaloblastic Recombinases Cell Line Gypsies Hemoglobins Infectious Anemia Virus, Equine Nijmegen Breakage Syndrome Pancytopenia Hematopoietic Stem Cells Oculocerebrorenal Syndrome Anemia, Refractory Nephrotic Syndrome HeLa Cells Basic-Leucine Zipper Transcription Factors Phenotype Sjogren's Syndrome Cell Line, Transformed Trioxsalen Molecular Sequence Data Nucleic Acid Synthesis Inhibitors DNA Breaks, Double-Stranded Sister Chromatid Exchange Fibroblasts DNA Replication Methoxsalen Anemia, Hemolytic, Congenital Lymphocytes Jews Ataxia Telangiectasia Mutated Proteins DNA Protein Binding DNA Repair-Deficiency Disorders Genes, Recessive Recombination, Genetic Equine Infectious Anemia Erythropoietin Alkylating Agents RecQ Helicases

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