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Translocation, Genetic
A type of chromosome aberration characterized by CHROMOSOME BREAKAGE and transfer of the broken-off portion to another location, often to a different chromosome.
推出的年份: 2005(1968)
副标题
drug effects
ethics
genetics
immunology
physiology
radiation effects
树号:
C23.550.210.870, G05.365.590.175.870, G05.558.860
MeSH 单一 ID:
D014178
进入的组:
Genetic Translocation
Genetic Translocations
Translocations, Genetic
Chromosomal Translocation
Chromosomal Translocations
Translocations, Chromosomal
Translocation, Chromosomal
早前的内容:
Chromosome Aberrations (1968-1974)
Chromosome Abnormalities (1966-1967)
All MeSH Categories
Diseases Category
Pathological Conditions, Signs and Symptoms [C23]
Pathologic Processes [C23.550]
Chromosome Aberrations [C23.550.210]
Abnormal Karyotype [C23.550.210.024]
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Aneuploidy [C23.550.210.050]
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Chromosomal Instability [C23.550.210.110]
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Chromosome Breakage [C23.550.210.170]
Chromosome Duplication [C23.550.210.182]
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Chromosome Inversion [C23.550.210.190]
Chromothripsis [C23.550.210.310]
Isochromosomes [C23.550.210.430]
Micronuclei, Chromosome-Defective [C23.550.210.570]
Nondisjunction, Genetic [C23.550.210.645]
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Polyploidy [C23.550.210.702]
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Ring Chromosomes [C23.550.210.760]
Sex Chromosome Aberrations [C23.550.210.815]
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Translocation, Genetic [C23.550.210.870]
Philadelphia Chromosome [C23.550.210.870.680]
All MeSH Categories
Phenomena and Processes
Genetic Phenomena [G05]
Genetic Variation [G05.365]
Mutation [G05.365.590]
Chromosome Aberrations [G05.365.590.175]
Abnormal Karyotype [G05.365.590.175.024]
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Aneuploidy [G05.365.590.175.050]
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Chimerism [G05.365.590.175.125]
Chromosomal Instability [G05.365.590.175.165]
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Chromosome Breakage [G05.365.590.175.175]
Chromosome Duplication [G05.365.590.175.183]
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Chromosome Inversion [G05.365.590.175.190]
Chromothripsis [G05.365.590.175.310]
Isochromosomes [G05.365.590.175.430]
Micronuclei, Chromosome-Defective [G05.365.590.175.570]
Mosaicism [G05.365.590.175.595]
Polyploidy [G05.365.590.175.677]
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Ring Chromosomes [G05.365.590.175.760]
Sex Chromosome Aberrations [G05.365.590.175.815]
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Translocation, Genetic [G05.365.590.175.870]
Philadelphia Chromosome [G05.365.590.175.870.680]
Uniparental Disomy [G05.365.590.175.935]
All MeSH Categories
Phenomena and Processes
Genetic Phenomena [G05]
Mutagenesis [G05.558]
Amino Acid Substitution [G05.558.109]
Chromosome Duplication [G05.558.164]
DNA Repeat Expansion [G05.558.220]
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Gene Amplification [G05.558.315]
Gene Duplication [G05.558.320]
INDEL Mutation [G05.558.370]
Mutagenesis, Insertional [G05.558.550]
Nondisjunction, Genetic [G05.558.620]
Sequence Deletion [G05.558.800]
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Sequence Inversion [G05.558.805]
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Somatic Hypermutation, Immunoglobulin [G05.558.810]
Suppression, Genetic [G05.558.835]
Translocation, Genetic [G05.558.860]
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