Chủ đề nóng: Phương pháp kỷ luật tích cực - Cổ học tinh hoa - Những thói hư tật xấu của người Việt - Công lý: Việc đúng nên làm - Giáo án Điện tử - Sách giáo khoa - Học tiếng Anh - Bài giảng trực tuyến - Món ăn bài thuốc - Chăm sóc bà bầu - Môi trường - Tiết kiệm điện - Nhi khoa - Ung thư - Tác hại của thuốc lá - Các kỹ thuật dạy học tích cực
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List of MeSH codes (G13)
Từ VLOS
- For other categories, see List of MeSH codes.
The following is a list of the "G" codes for MeSH. It is a product of the United States National Library of Medicine.
Source for content is here. (File "2006 MeSH Trees".)
Mục lục
-
1
MeSH
G13
---
genetic
phenomena
- 1.1 MeSH G13.180 --- consanguinity
- 1.2 MeSH G13.285 --- founder effect
- 1.3 MeSH G13.330 --- gene frequency
- 1.4 MeSH G13.340 --- gene order
- 1.5 MeSH G13.345 --- gene pool
- 1.6 MeSH G13.360 --- genetic load
- 1.7 MeSH G13.370 --- genomic instability
- 1.8 MeSH G13.380 --- genotype
- 1.9 MeSH G13.400 --- hybrid vigor
- 1.10 MeSH G13.420 --- inheritance patterns
- 1.11 MeSH G13.540 --- linkage (genetics)
- 1.12 MeSH G13.695 --- phenotype
- 1.13 MeSH G13.697 --- phylogeny
- 1.14 MeSH G13.700 --- ploidies
- 1.15 MeSH G13.810 --- sequence homology
- 1.16 MeSH G13.815 --- sex ratio
- 1.17 MeSH G13.820 --- structural homology, protein
- 1.18 MeSH G13.920 --- variation (genetics)
MeSH G13 --- genetic phenomena[sửa]
MeSH G13.180 --- consanguinity[sửa]
MeSH G13.285 --- founder effect[sửa]
MeSH G13.330 --- gene frequency[sửa]
- MeSH G13.330.159 --- gene flow
- MeSH G13.330.320 --- genetic drift
MeSH G13.340 --- gene order[sửa]
MeSH G13.345 --- gene pool[sửa]
MeSH G13.360 --- genetic load[sửa]
MeSH G13.370 --- genomic instability[sửa]
MeSH G13.380 --- genotype[sửa]
- MeSH G13.380.350 --- gene dosage
- MeSH G13.380.355 --- genetic predisposition to disease
- MeSH G13.380.360 --- haplotypes
- MeSH G13.380.383 --- heterozygote
- MeSH G13.380.554 --- homozygote
MeSH G13.400 --- hybrid vigor[sửa]
MeSH G13.420 --- inheritance patterns[sửa]
- MeSH G13.420.040 --- anticipation, genetic
- MeSH G13.420.275 --- extrachromosomal inheritance
- MeSH G13.420.275.500 --- genes, mitochondrial
- MeSH G13.420.320 --- genes, dominant
- MeSH G13.420.325 --- genes, recessive
- MeSH G13.420.457 --- genes, x-linked
- MeSH G13.420.523 --- genes, y-linked
- MeSH G13.420.590 --- multifactorial inheritance
- MeSH G13.420.720 --- quantitative trait, heritable
MeSH G13.540 --- linkage (genetics)[sửa]
MeSH G13.695 --- phenotype[sửa]
MeSH G13.697 --- phylogeny[sửa]
MeSH G13.700 --- ploidies[sửa]
- MeSH G13.700.131 --- aneuploidy
- MeSH G13.700.131.500 --- monosomy
- MeSH G13.700.131.750 --- trisomy
- MeSH G13.700.264 --- diploidy
- MeSH G13.700.456 --- haploidy
- MeSH G13.700.740 --- polyploidy
MeSH G13.810 --- sequence homology[sửa]
- MeSH G13.810.200 --- sequence homology, amino acid
- MeSH G13.810.550 --- sequence homology, nucleic acid
- MeSH G13.810.550.830 --- synteny
MeSH G13.815 --- sex ratio[sửa]
MeSH G13.820 --- structural homology, protein[sửa]
MeSH G13.920 --- variation (genetics)[sửa]
- MeSH G13.920.036 --- antibody diversity
- MeSH G13.920.073 --- antigenic variation
- MeSH G13.920.331 --- genetic heterogeneity
- MeSH G13.920.590 --- mutation
- MeSH G13.920.590.029 --- allelic imbalance
- MeSH G13.920.590.029.530 --- loss of heterozygosity
- MeSH G13.920.590.029.530.175 --- chromosome deletion
- MeSH G13.920.590.060 --- base pair mismatch
- MeSH G13.920.590.120 --- codon, nonsense
- MeSH G13.920.590.175 --- chromosome aberrations
- MeSH G13.920.590.175.050 --- aneuploidy
- MeSH G13.920.590.175.050.500 --- monosomy
- MeSH G13.920.590.175.050.750 --- trisomy
- MeSH G13.920.590.175.125 --- chimerism
- MeSH G13.920.590.175.165 --- chromosomal instability
- MeSH G13.920.590.175.165.180 --- chromosome fragility
- MeSH G13.920.590.175.175 --- chromosome breakage
- MeSH G13.920.590.175.177 --- chromosome deletion
- MeSH G13.920.590.175.420 --- inversion, chromosome
- MeSH G13.920.590.175.430 --- isochromosomes
- MeSH G13.920.590.175.570 --- micronuclei, chromosome-defective
- MeSH G13.920.590.175.595 --- mosaicism
- MeSH G13.920.590.175.760 --- ring chromosomes
- MeSH G13.920.590.175.815 --- sex chromosome aberrations
- MeSH G13.920.590.175.815.970 --- xyy karyotype
- MeSH G13.920.590.175.870 --- translocation, genetic
- MeSH G13.920.590.175.870.680 --- philadelphia chromosome
- MeSH G13.920.590.175.935 --- uniparental disomy
- MeSH G13.920.590.220 --- dna repeat expansion
- MeSH G13.920.590.220.865 --- trinucleotide repeat expansion
- MeSH G13.920.590.300 --- frameshift mutation
- MeSH G13.920.590.310 --- gene amplification
- MeSH G13.920.590.320 --- gene duplication
- MeSH G13.920.590.335 --- genomic instability
- MeSH G13.920.590.350 --- germ-line mutation
- MeSH G13.920.590.650 --- mutation, missense
- MeSH G13.920.590.675 --- point mutation
- MeSH G13.920.590.762 --- sequence deletion
- MeSH G13.920.590.762.180 --- chromosome deletion
- MeSH G13.920.590.762.320 --- gene deletion
- MeSH G13.920.590.835 --- suppression, genetic
- MeSH G13.920.795 --- polymorphism, genetic
- MeSH G13.920.795.595 --- polymorphism, restriction fragment length
- MeSH G13.920.795.600 --- polymorphism, single-stranded conformational
- MeSH G13.920.795.800 --- polymorphism, single nucleotide