Medical Subject Headings
MeSH Tree Structures - 2008
G13 - Genetic Phenomena
- Genetic Phenomena [G13]
- Consanguinity [G13.180]
- Founder Effect [G13.285]
- Gene Frequency [G13.330]
- Gene Order [G13.340]
- Gene Pool [G13.345]
- Genetic Load [G13.360]
- Genomic Instability [G13.370]
- Genotype [G13.380]
- Hybrid Vigor [G13.400]
- Inheritance Patterns [G13.420]
- Linkage (Genetics) [G13.540]
- Phenotype [G13.695]
- Phylogeny [G13.697]
- Ploidies [G13.700]
- Sequence Homology [G13.810]
- Sex Ratio [G13.815]
- Structural Homology, Protein [G13.820]
- Variation (Genetics) [G13.920]
- Antibody Diversity [G13.920.036]
- Antigenic Variation [G13.920.073]
- Genetic Heterogeneity [G13.920.331]
- Mutation [G13.920.590]
- Allelic Imbalance [G13.920.590.029]
- Base Pair Mismatch [G13.920.590.060]
- Chromosome Aberrations [G13.920.590.175]
- Aneuploidy [G13.920.590.175.050]
- Chimerism [G13.920.590.175.125]
- Chromosomal Instability [G13.920.590.175.165]
- Chromosome Breakage [G13.920.590.175.175]
- Chromosome Deletion [G13.920.590.175.177]
- Inversion, Chromosome [G13.920.590.175.420]
- Isochromosomes [G13.920.590.175.430]
- Micronuclei, Chromosome-Defective [G13.920.590.175.570]
- Mosaicism [G13.920.590.175.595]
- Ring Chromosomes [G13.920.590.175.760]
- Sex Chromosome Aberrations [G13.920.590.175.815]
- Translocation, Genetic [G13.920.590.175.870]
- Uniparental Disomy [G13.920.590.175.935]
- Codon, Nonsense [G13.920.590.195]
- DNA Repeat Expansion [G13.920.590.220]
- Frameshift Mutation [G13.920.590.265]
- Gene Amplification [G13.920.590.310]
- Gene Duplication [G13.920.590.320]
- Genomic Instability [G13.920.590.335]
- Germ-Line Mutation [G13.920.590.350]
- INDEL Mutation [G13.920.590.500]
- Mutagenesis, Insertional [G13.920.590.575]
- Mutation, Missense [G13.920.590.650]
- Point Mutation [G13.920.590.675]
- Sequence Deletion [G13.920.590.762]
- Suppression, Genetic [G13.920.590.835]
- Polymorphism, Genetic [G13.920.795]
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